EP3225185B1 - Système d'agrafage chirurgical comprenant un mécanisme de transmission réglable - Google Patents

Système d'agrafage chirurgical comprenant un mécanisme de transmission réglable Download PDF

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Publication number
EP3225185B1
EP3225185B1 EP17164412.3A EP17164412A EP3225185B1 EP 3225185 B1 EP3225185 B1 EP 3225185B1 EP 17164412 A EP17164412 A EP 17164412A EP 3225185 B1 EP3225185 B1 EP 3225185B1
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European Patent Office
Prior art keywords
staple
drive
staples
anvil
shaft
Prior art date
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EP17164412.3A
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German (de)
English (en)
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EP3225185A3 (fr
EP3225185A2 (fr
Inventor
Iv Frederick E. Shelton
Adam D. HENSEL
Shailendra K. Parihar
Pinaki Mukherjee
Jason L. Harris
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Ethicon LLC
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Ethicon LLC
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Priority claimed from US15/089,312 external-priority patent/US11284890B2/en
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Publication of EP3225185A3 publication Critical patent/EP3225185A3/fr
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    • A61B2017/2912—Handles transmission of forces to actuating rod or piston
    • A61B2017/2919—Handles transmission of forces to actuating rod or piston details of linkages or pivot points
    • A61B2017/2922—Handles transmission of forces to actuating rod or piston details of linkages or pivot points toggle linkages
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/28—Surgical forceps
    • A61B17/29—Forceps for use in minimally invasive surgery
    • A61B17/2909—Handles
    • A61B2017/2912—Handles transmission of forces to actuating rod or piston
    • A61B2017/2923—Toothed members, e.g. rack and pinion
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61B17/28—Surgical forceps
    • A61B17/29—Forceps for use in minimally invasive surgery
    • A61B2017/2926—Details of heads or jaws
    • A61B2017/2927—Details of heads or jaws the angular position of the head being adjustable with respect to the shaft
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/28—Surgical forceps
    • A61B17/29—Forceps for use in minimally invasive surgery
    • A61B2017/2926—Details of heads or jaws
    • A61B2017/2932—Transmission of forces to jaw members
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/28—Surgical forceps
    • A61B17/29—Forceps for use in minimally invasive surgery
    • A61B2017/2946—Locking means
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/03—Automatic limiting or abutting means, e.g. for safety
    • A61B2090/033—Abutting means, stops, e.g. abutting on tissue or skin
    • A61B2090/034—Abutting means, stops, e.g. abutting on tissue or skin abutting on parts of the device itself
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/08—Accessories or related features not otherwise provided for
    • A61B2090/0801—Prevention of accidental cutting or pricking
    • A61B2090/08021—Prevention of accidental cutting or pricking of the patient or his organs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/08—Accessories or related features not otherwise provided for
    • A61B2090/0807—Indication means
    • A61B2090/0808—Indication means for indicating correct assembly of components, e.g. of the surgical apparatus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/08—Accessories or related features not otherwise provided for
    • A61B2090/0807—Indication means
    • A61B2090/0811—Indication means for the position of a particular part of an instrument with respect to the rest of the instrument, e.g. position of the anvil of a stapling instrument
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/08—Accessories or related features not otherwise provided for
    • A61B2090/0814—Preventing re-use
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/36—Image-producing devices or illumination devices not otherwise provided for
    • A61B90/37—Surgical systems with images on a monitor during operation

Definitions

  • the present invention relates to surgical instruments and, in various arrangements, to surgical stapling and cutting instruments and staple cartridges for use therewith that are designed to staple and cut tissue.
  • US 2014/305991 A1 relates to a drive system for a surgical instrument.
  • the system can comprise a drive assembly, a first output assembly, and a second output assembly.
  • the drive assembly can be coupled to a motor, and can operably transmit a force from the motor to the first output assembly and/or the second output assembly.
  • the drive system can further comprise a shifter assembly, which can shift engagement of the drive assembly between the first output assembly and the second output assembly.
  • proximal and distal are used herein with reference to a clinician manipulating the handle portion of the surgical instrument.
  • proximal refers to the portion closest to the clinician and the term “distal” refers to the portion located away from the clinician.
  • distal refers to the portion located away from the clinician.
  • spatial terms such as “vertical”, “horizontal”, “up”, and “down” may be used herein with respect to the drawings.
  • surgical instruments are used in many orientations and positions, and these terms are not intended to be limiting and/or absolute.
  • Various exemplary devices and methods are provided for performing laparoscopic and minimally invasive surgical procedures.
  • the various methods and devices disclosed herein can be used in numerous surgical procedures and applications including, for example, in connection with open surgical procedures.
  • the various instruments disclosed herein can be inserted into a body in any way, such as through a natural orifice, through an incision or puncture hole formed in tissue, etc.
  • the working portions or end effector portions of the instruments can be inserted directly into a patient's body or can be inserted through an access device that has a working channel through which the end effector and elongate shaft of a surgical instrument can be advanced.
  • a surgical stapling system can comprise a shaft and an end effector extending from the shaft.
  • the end effector comprises a first jaw and a second jaw.
  • the first jaw comprises a staple cartridge.
  • the staple cartridge is insertable into and removable from the first jaw; however, other embodiments are envisioned in which a staple cartridge is not removable from, or at least readily replaceable from, the first jaw.
  • the second jaw comprises an anvil configured to deform staples ejected from the staple cartridge.
  • the second jaw is pivotable relative to the first jaw about a closure axis; however, other embodiments are envisioned in which first jaw is pivotable relative to the second jaw.
  • the surgical stapling system further comprises an articulation joint configured to permit the end effector to be rotated, or articulated, relative to the shaft.
  • the end effector is rotatable about an articulation axis extending through the articulation joint. Other embodiments are envisioned which do not include an articulation joint.
  • the staple cartridge comprises a cartridge body.
  • the cartridge body includes a proximal end, a distal end, and a deck extending between the proximal end and the distal end.
  • the staple cartridge is positioned on a first side of the tissue to be stapled and the anvil is positioned on a second side of the tissue.
  • the anvil is moved toward the staple cartridge to compress and clamp the tissue against the deck.
  • staples removably stored in the cartridge body can be deployed into the tissue.
  • the cartridge body includes staple cavities defined therein wherein staples are removably stored in the staple cavities.
  • the staple cavities are arranged in six longitudinal rows. Three rows of staple cavities are positioned on a first side of a longitudinal slot and three rows of staple cavities are positioned on a second side of the longitudinal slot. Other arrangements of staple cavities and staples may be possible.
  • the staples are supported by staple drivers in the cartridge body.
  • the drivers are movable between a first, or unfired position, and a second, or fired, position to eject the staples from the staple cavities.
  • the drivers are retained in the cartridge body by a retainer which extends around the bottom of the cartridge body and includes resilient members configured to grip the cartridge body and hold the retainer to the cartridge body.
  • the drivers are movable between their unfired positions and their fired positions by a sled.
  • the sled is movable between a proximal position adjacent the proximal end and a distal position adjacent the distal end.
  • the sled comprises a plurality of ramped surfaces configured to slide under the drivers and lift the drivers, and the staples supported thereon, toward the anvil.
  • the sled is moved distally by a firing member.
  • the firing member is configured to contact the sled and push the sled toward the distal end.
  • the longitudinal slot defined in the cartridge body is configured to receive the firing member.
  • the anvil also includes a slot configured to receive the firing member.
  • the firing member further comprises a first cam which engages the first jaw and a second cam which engages the second jaw. As the firing member is advanced distally, the first cam and the second cam can control the distance, or tissue gap, between the deck of the staple cartridge and the anvil.
  • the firing member also comprises a knife configured to incise the tissue captured intermediate the staple cartridge and the anvil. It is desirable for the knife to be positioned at least partially proximal to the ramped surfaces such that the staples are ejected ahead of the knife.
  • FIG. 1 depicts a motor-driven surgical system 10 that may be used to perform a variety of different surgical procedures.
  • the motor driven surgical system 10 comprises a selectively reconfigurable housing or handle assembly 20 that is attached to one form of an interchangeable surgical tool assembly 1000.
  • the system 10 that is depicted in FIG. 1 includes an interchangeable surgical tool assembly 1000 that comprises a surgical cutting and fastening instrument which may be referred to as an endocutter.
  • the interchangeable surgical tool assemblies may include end effectors that are adapted to support different sizes and types of staple cartridges and, have different shaft lengths, sizes, and types, etc. Such arrangements, for example, may utilize any suitable fastener, or fasteners, to fasten tissue.
  • a fastener cartridge comprising a plurality of fasteners removably stored therein can be removably inserted into and/or attached to the end effector of a surgical tool assembly.
  • Other surgical tool assemblies may be interchangeably employed with the handle assembly 20.
  • the interchangeable surgical tool assembly 1000 may be detached from the handle assembly 20 and replaced with a different surgical tool assembly that is configured to perform other surgical procedures.
  • the surgical tool assembly may not be interchangeable with other surgical tool assemblies and essentially comprise a dedicated shaft that is non-removably affixed or coupled to the handle assembly 20, for example.
  • the surgical tool assemblies may also be referred to as elongate shaft assemblies.
  • the surgical tool assemblies may be reusable or, in other configurations, the surgical tool assemblies may be designed to be disposed of after a single use.
  • housing and “housing assembly” may also encompass a housing or similar portion of a robotic system that houses or otherwise operably supports at least one drive system that is configured to generate and apply at least one control motion which could be used to actuate the elongate shaft assemblies disclosed herein and their respective equivalents.
  • frame may refer to a portion of a handheld surgical instrument.
  • frame may also represent a portion of a robotically controlled surgical instrument and/or a portion of the robotic system that may be used to operably control a surgical instrument.
  • the surgical tool assemblies disclosed herein may be employed with various robotic systems, instruments, components and methods such as, but not limited to, those disclosed in U.S. Patent Application Serial No. 13/118,241 , entitled SURGICAL STAPLING INSTRUMENTS WITH ROTATABLE STAPLE DEPLOYMENT ARRANGEMENTS, now U.S. Patent Application Publication No. 2012/0298719 .
  • the housing assembly or handle assembly 20 comprises a primary housing portion 30 that may be formed from a pair of housing segments 40, 70 that may be fabricated from plastic, polymer materials, metal, etc. and be joined together by an appropriate fastener arrangement such as, for example, adhesive, screws, press-fit features, snap-fit features, latches, etc.
  • the primary housing portion 30 operably supports a plurality of drive systems therein that are configured to generate and apply various control motions to corresponding portions of the interchangeable surgical tool assembly that is operably attached thereto.
  • the handle assembly 20 further comprises a grip portion 100 that is movably coupled to the primary housing portion 30 and is configured to be gripped and manipulated by the clinician in various positions relative to the primary housing portion 30.
  • the grip portion 100 may be fabricated from a pair of grip segments 110, 120 that may be fabricated from plastic, polymer materials, metal, etc. and are joined together by an appropriate fastener arrangement such as, for example, adhesive, screws, press-fit features, snap-fit features, latches, etc. for assembly and maintenance purposes.
  • the grip portion 100 comprises a grip housing 130 that defines a hollow cavity 132 that is configured to operably support a drive motor and gearbox which will be discussed in further detail below.
  • the upper portion 134 of the grip housing 130 is configured to extend through an opening 80 in the primary housing portion 30 and be pivotally journaled on a pivot shaft 180.
  • the pivot shaft 180 defines a pivot axis designated as "PA”. See FIG. 3 .
  • the handle assembly 20 defines a handle axis designated as "HA" that may be parallel to the shaft axis "SA” of the elongate shaft assembly of the interchangeable surgical tool that is operably attached to the handle assembly 20.
  • the pivot axis PA is transverse to the handle axis HA. See FIG.
  • the grip housing 130 defines a grip axis, generally designated as "GA". See FIG. 2 .
  • the clinician might want to position the grip portion 100 relative to the primary housing portion 30 such that the grip axis GA is perpendicular or approximately perpendicular (angle "HI") to the handle axis HA (referred to herein as a "first grip position"). See FIG. 5 .
  • the clinician may wish to pivot the grip portion 100 relative to the primary housing portion 30 to a position wherein the grip axis GA is at a forty-five degree or approximately forty-five degree angle or other suitable acute angle (angle "H2") relative to the handle axis HA.
  • This position is referred to herein as a "second grip position".
  • FIG. 5 illustrates the grip portion 100 in phantom lines in the second grip position.
  • the handle assembly 20 also includes a grip locking system, generally designated as 150, for selectively locking the grip portion 100 in the desired orientation relative to the primary housing portion 30.
  • the grip locking system 150 comprises an arcuate series 152 of pointed teeth 154.
  • the teeth 154 are spaced from each other and form a locking groove 156 therebetween.
  • Each locking groove 156 corresponds to a particular angular locking position for the grip portion 100.
  • the teeth 154 and locking grooves or "locking locations" 156 are arranged to permit the grip portion 100 to be locked at 10-15 degree intervals between the first grip position and the second grip position.
  • the arrangement may employ two stop positions which are tailored to the type of instrument (shaft arrangement) employed.
  • the grip locking system 150 further includes a locking button 160 that has a locking portion that is configured to lockingly engage the locking grooves 156.
  • the locking button 160 is pivotally mounted in the primary handle portion 30 on a pivot pin 131 to permit the locking button 160 to pivot into engagement with a corresponding locking groove 156.
  • a locking spring 164 serves to bias the locking button 160 into an engaged or locked position with the corresponding locking groove 156.
  • the locking portion and the teeth configurations serve to enable the teeth 154 to slide past the locking portion when the clinician depresses the locking button 160.
  • the clinician depresses the locking button 160 and then pivots the grip portion 100 to the desired angular position. Once the grip portion 100 has been moved to the desired position, the clinician releases the locking button 160. The locking spring 164 will then bias the locking button 160 toward the series of teeth 154 so that the locking portion enters the corresponding locking groove 156 to retain the grip portion 100 in that position during use.
  • the handle assembly 20 operably supports a first rotary drive system 300, a second rotary drive system 320 and a third axial drive system 400.
  • the rotary drive systems 300, 320 are each powered by a motor 200 that is operably supported in the grip portion 100.
  • the motor 200 is supported within the cavity 132 in the grip portion 100 and has a gear box assembly 202 that has an output drive shaft 204 protruding therefrom.
  • the motor 200 may be a DC brushed driving motor having a maximum rotation of, approximately, 25,000 RPM, for example.
  • the motor may include a brushless motor, a cordless motor, a synchronous motor, a stepper motor, or any other suitable electric motor.
  • the motor 200 may be powered by a power source 210 that, in one form, may comprise a removable power pack 212.
  • the power source 210 may comprise, for example, anyone of the various power source arrangements disclosed in further detail in U.S. Patent Application Publication No. 2015/0272575 and entitled SURGICAL INSTRUMENT COMPRISING A SENSOR SYSTEM .
  • the power pack 212 may comprise a proximal housing portion 214 that is configured for attachment to a distal housing portion 216.
  • the proximal housing portion 214 and the distal housing portion 216 are configured to operably support a plurality of batteries 218 therein.
  • Batteries 218 may each comprise, for example, a Lithium Ion ("LI”) or other suitable battery.
  • LI Lithium Ion
  • the distal housing portion 216 is configured for removable operable attachment to a handle circuit board assembly 220 which is also operably coupled to the motor 200.
  • the handle circuit board assembly 220 may also be generally referred to herein as the "control system or CPU 224".
  • a number of batteries 218 may be connected in series may be used as the power source for the handle assembly 20.
  • the power source 210 may be replaceable and/or rechargeable.
  • the surgical instrument 10 may be powered by alternating current (AC) for example.
  • the motor 200 may be controlled by a rocker switch 206 that is mounted to the grip portion 100.
  • the motor 200 is operably coupled to a gear box assembly 202 that includes an output drive shaft 204. Attached to the output drive shaft 204 is a driver bevel gear 230.
  • the motor 200, the gear box assembly 202, the output drive shaft 204 and the driver bevel gear 230 may also be collectively referred to herein as a "motor assembly 231".
  • the driver bevel gear 230 interfaces with a driven bevel gear 234 that is attached to a system drive shaft 232 as well as a pivot bevel gear 238 that is journaled on the pivot shaft 180.
  • the driven bevel gear 234 is axially movable on the system drive shaft 232 between an engaged position wherein the driven bevel gear 234 is in meshing engagement with the driver bevel gear 230 ( FIG. 5 ) and a disengaged position wherein the driven bevel gear 234 is out of meshing engagement with the drive bevel gear 230 ( FIG. 14 ).
  • a drive system spring 235 is journaled between the driven bevel gear 234 and a proximal end flange 236 that is formed on a proximal portion ofthe system drive shaft 232. See FIGS. 4 and 14 .
  • the drive system spring 235 serves to bias the driven bevel gear 234 out of meshing engagement with the driver bevel gear 230 as will be discussed in further detail below.
  • the pivot bevel gear 238 facilitates pivotal travel of the output drive shaft 204 and driver bevel gear 230 with the grip portion 100 relative to the primary handle portion 30.
  • the system drive shaft 232 interfaces with a rotary drive selector system, generally designated as 240.
  • the rotary drive selector system 240 comprises a shifter gear 250 that is selectively movable between the first rotary drive system 300 and the second rotary drive system 320.
  • the drive selector system 240 comprises a shifter mounting plate 242 that is non-movably mounted within primary handle portion 30.
  • the shifter mounting plate 242 may be frictionally retained between mounting lugs (not shown) formed in the housing segments 40, 70 or be otherwise retained therein by screws, adhesive, etc. Still referring to FIGS.
  • the system drive shaft 232 extends through a hole in the shifter mounting plate 242 and has the central, or system, drive gear 237 non-rotatably attached thereto.
  • the central drive gear 237 may be attached to the system drive shaft 232 by a keyway arrangement 233. See FIGS. 6-9 .
  • the system drive shaft 232 may be rotatably supported in the shifter mounting plate 242 by a corresponding bearing (not shown) that is mounted thereto. In any event, rotation of the system drive shaft 232 will result in rotation of the central drive gear 234.
  • the first drive system 300 includes a first drive socket 302 that is rotatably supported in a distal wall 32 formed in the primary handle portion 30.
  • the first drive socket 302 may comprise a first body portion 304 that has a splined socket formed therein.
  • a first driven gear 306 is formed on or is non-movably attached to the first body portion 304.
  • the first body portion 304 may be rotatably supported in a corresponding hole or passage provided the distal wall 32 or it may be rotatably supported in a corresponding bearing (not shown) that is mounted in the distal wall 32.
  • the second rotary drive system 320 includes a second drive socket 322 that is also rotatably supported in the distal wall 32 of the primary handle portion 30.
  • the second drive socket 322 may comprise a second body portion 324 that has a splined socket formed therein.
  • a second driven gear 326 is formed on or is non-rotatably mounted to the second body portion 324.
  • the second body portion 324 may be rotatably supported in a corresponding hole or passage provided the distal wall 32 or it may be rotatably supported in a corresponding bearing (not shown) that is mounted in the distal wall 32.
  • the first and second drive sockets 302, 322 are spaced from each other on each lateral side of the handle axis HA. See FIG. 4 , for example.
  • the rotary drive selector system 240 includes a shifter gear 250.
  • the shifter gear 250 is rotatably mounted on an idler shaft 252 that is movably supported in an arcuate slot 244 in the shifter mounting plate 242.
  • the shifter gear 250 is mounted so as to freely rotate on the idler shaft 252 and remain in meshing engagement with the central drive gear 234.
  • the idler shaft 252 is coupled to an end of a shaft 262 of a shifter solenoid 260.
  • the shifter solenoid 260 is pinned or otherwise mounted with the primary handle housing 30 such that when the shifter solenoid 260 is actuated, the shifter gear 250 is moved into meshing engagement with one of the first driven gear 306 or the second driven gear 326.
  • the shifter gear 250 is in meshing engagement with the central drive gear 234 and the first driven gear 306 such that actuation of the motor 200 will result in rotation of the first drive socket 302.
  • a shifter spring 266 may be employed to bias the shifter gear 250 into that first actuation position.
  • the shifter spring 266 will automatically bias the shifter gear 250 into the first position.
  • the shifter gear 250 is in that position, subsequent actuation of the motor 200 will result in rotation of the first drive socket 302 of the first rotary drive system 300.
  • the shifter solenoid is actuated, the shifter gear 250 is moved into meshing engagement with the second driven gear 326 on the second drive socket 322. Thereafter, actuation of the motor 200 will result in actuation or rotation of the second drive socket 322 of the second rotary drive system 320.
  • the first and second rotary drive systems 300, 320 may be used to power various component portions of the interchangeable surgical tool assembly that is coupled thereto.
  • the shifter spring 266 will bias the shifter gear 250 to the first position.
  • the handle assembly 20 of the illustrated example employs a manually actuatable "bailout" system, generally designated as 330, for manually applying a rotary drive motion to the first rotary drive system 300 in the above described scenario, for example.
  • the illustrated bailout system 330 comprises a bailout drive train 332 that includes a planetary gear assembly 334.
  • the planetary gear assembly 334 includes a planetary gear housing 336 that houses a planetary gear arrangement (not shown) that includes a planetary bevel gear 338.
  • the planetary gear assembly 334 includes a bailout drive shaft 340 that is operably coupled to the planetary gear arrangement within the planetary gear housing 336. Rotation of the planetary bevel gear 338 rotates the planetary gear arrangement which ultimately rotates the bailout drive shaft 340.
  • a bailout drive gear 342 is journaled on the bailout drive shaft 340 so that the bailout drive gear 342 can move axially on the bailout drive shaft 340, yet rotate therewith.
  • the bailout drive gear 342 is movable between a spring stop flange 344 that is formed on the bailout drive shaft 340 and a shaft end stop 346 that is formed on the distal end of the bailout drive shaft 340.
  • a bailout shaft spring 348 is journaled on the bailout drive shaft 340 between the bailout drive gear 342 and the spring stop flange 344.
  • the bailout shaft spring 348 biases the bailout drive gear 342 distally on the bailout drive shaft 340.
  • the bailout system 330 includes a bailout actuator assembly or bailout handle assembly 360 that facilitates the manual application of a bailout drive motion to the bailout drive train 332.
  • the bailout handle assembly 360 includes a bailout bevel gear assembly 362 that comprises a bailout bevel gear 364 and a ratchet gear 366.
  • the bailout handle assembly 360 further includes a bailout handle 370 that is movably coupled to the bailout bevel gear assembly 362 by a pivot yoke 372 that is pivotally mounted on the ratchet gear 366.
  • the bailout handle 370 is pivotally coupled to the pivot yoke 372 by a pin 374 for selective pivotal travel between a stored position "SP" and an actuation position "AP". See FIG. 12 .
  • a handle spring 376 is employed to bias the bailout handle 370 into the actuation position AP.
  • the angle between the axis SP representing the stored position and the axis AP representing the actuation position may be approximately thirty degrees, for example. See FIG. 13 .
  • the bailout handle assembly 360 further includes a ratchet pawl 378 that is rotatably mounted in a cavity or hole 377 in the pivot yoke 372.
  • the ratchet pawl 378 is configured to meshingly engage the ratchet gear 366 when rotated in an actuation direction "AD" and then rotate out of meshing engagement when rotated in the opposite direction.
  • a ratchet spring 384 and ball member 386 are movably supported in a cavity 379 in the pivot yoke 372 and serve to lockingly engage detents 380, 382 in the ratchet pawl 378 as the bailout handle 370 is actuated (ratcheted).
  • the bailout system 330 further includes a bailout access panel 390 that is maneuverable between an open position and a closed position.
  • the bailout access panel 390 is configured to be removably coupled to the housing segment 70 of the primary housing portion 30.
  • the bailout access panel 390 when the bailout access panel 390 is removed or detached from the primary housing portion 30, it is said to be in an "open” position and when the bailout access panel 390 is attached to the primary housing portion 30 as illustrated, it is said to be in a "closed” position.
  • Other embodiments are contemplated, however, wherein the access panel is movably coupled to the primary housing portion such that when the access panel is in the open position, it remains attached thereto.
  • the access panel may be pivotally attached to the primary housing portion or slidably attached to the primary housing portion and be maneuverable between an open position and a closed position.
  • the bailout access panel 390 is configured to snappingly engage corresponding portions of the housing segment 70 to removably retain it in a "closed" position.
  • Other forms of mechanical fasteners such as screws, pins, etc. could also be used.
  • the bailout access panel 390 includes a drive system locking member or yoke 392 and a bailout locking member or yoke 396 that each protrudes out from the backside thereof or are otherwise formed thereon.
  • the drive system locking yoke 392 includes a drive shaft notch 394 that is configured to receive a portion of the system drive shaft 232 therein when the bailout access panel 390 is installed in the primary housing portion 30 (i.e., the bailout access panel is in the "closed" position).
  • the drive system locking yoke 392 serves to bias the driven bevel gear 234 into meshing engagement with the driver bevel gear 230 (against the bias of the drive system spring 235).
  • the bailout locking yoke 396 includes a bailout drive shaft notch 397 that is configured to receive a portion of the bailout drive shaft 340 therein when the bailout access panel 390 is installed or positioned in the closed position.
  • the bailout locking yoke 396 also serves to bias the bailout drive gear 342 out of meshing engagement with the bailout driven gear 350 (against the bias of the bailout shaft spring 348).
  • the bailout locking yoke 396 prevents the bailout drive gear 342 from interfering with rotation of the system drive shaft 232 when the bailout access panel 390 is installed or in the closed position.
  • the bailout locking yoke 396 includes a handle notch 398 for engaging the bailout handle 370 and retaining it in the stored position SP.
  • FIGS. 4 , 5 and 10 illustrate the configurations of the drive system components and the bailout system components when the bailout access panel 390 is installed or is in the closed position.
  • the drive system locking member 392 biases the driven bevel gear 234 into meshing engagement with the driver bevel gear 230.
  • actuation of the motor 200 will result in the rotation of the driver bevel gear 230 and ultimately the system drive shaft 232.
  • the bailout locking yoke 396 serves to bias the bailout drive gear 342 out of meshing engagement with the bailout driven gear 350 on the system drive shaft 232.
  • the drive system is actuatable by the motor 200 and the bailout system 330 is disconnected or prevented from applying any actuation motion to the system drive shaft 232.
  • the clinician first removes the bailout access panel 390 or otherwise moves the bailout access panel 390 to the open position. This action removes the drive system locking member 392 from engagement with the driven bevel gear 234 which thereby permits the drive system spring 235 to bias the driven bevel gear 234 out of meshing engagement with the driver bevel gear 230.
  • the clinician can manually ratchet the bailout handle 370 in the ratchet directions RD which results in the rotation of the of the ratchet bevel gear 364 (in a clockwise direction in FIG. 14 , for example) which ultimately results in the application of a retraction rotary motion to the system drive shaft 232 through the bailout drive train 332.
  • the clinician may ratchet the bailout handle 370 a number of times until the system drive shaft 232 has been sufficiently rotated a number of times to retract a component of the surgical end effector portion of the surgical tool assembly that is attached to the handle assembly 20.
  • the clinician may then replace the bailout access panel 390 (i.e., return the bailout access panel 390 to the closed position) to thereby cause the drive system locking member 392 to bias the driven bevel gear 234 into meshing engagement with the driver bevel gear 230 and the bailout locking yoke 396 to bias the bailout drive gear 342 out of meshing engagement with the bailout driven gear 350.
  • the shifter spring 266 will bias the shifter solenoid 260 into the first actuation position. As such, actuation of the bailout system 330 will result in the application of reversing or retraction motions to the first rotary drive system 300.
  • a surgical stapling instrument can comprise a manually-actuated bailout system configured to retract a staple firing drive, for example.
  • the bailout system may need to be operated and/or cranked more than one time to fully retract the staple firing drive.
  • the user of the stapling instrument may lose track of how many times they have cranked the bailout and/or otherwise become confused as to how much further the firing drive needs to be retracted.
  • the stapling instrument comprises a system configured to detect the position of a firing member of the firing drive, determine the distance in which the firing member needs to be retracted, and display that distance to the user of the surgical instrument.
  • a surgical stapling instrument comprises one or more sensors configured to detect the position of the firing member.
  • the sensors comprise Hall Effect sensors, for example, and can be positioned in a shaft and/or end effector of the stapling instrument.
  • the sensors are in signal communication with a controller of the surgical stapling instrument which is, in turn, in signal communication with a display on the surgical stapling instrument.
  • the controller comprises a microprocessor configured to compare the actual position of the firing member to a datum, or reference, position - which comprises a fully retracted position of the firing member - and calculate the distance, i.e., the remaining distance, between the actual position of the firing member and the reference position.
  • the display comprises an electronic display, for example, and the controller is configured to display the remaining distance on the electronic display in any suitable manner.
  • the controller displays a progress bar on the display.
  • an empty progress bar can represent that the firing member is at the end of its firing stroke and a full progress bar can represent that the firing member has been fully retracted, for example.
  • 0% can represent that the firing member is at the end of its firing stroke and 100% can represent that the firing member has been fully retracted, for example.
  • the controller is configured to display how many actuations of the bailout mechanism are required to retract the firing member to its fully retracted position on the display.
  • the actuation of the bailout mechanism can operably disconnect a battery, or power source, of the surgical stapling instrument from an electric motor of the firing drive.
  • the actuation of the bailout mechanism flips a switch which electrically decouples the battery from the electric motor. Such a system would prevent the electric motor from resisting the manual retraction of the firing member.
  • the illustrated handle assembly 20 also supports a third axial drive system that is generally designated as 400.
  • the third axial drive system 400 in at least one form, comprises a solenoid 402 that has a third drive actuator member or rod 410 protruding therefrom.
  • the distal end 412 of the third drive actuator member 410 has a third drive cradle or socket 414 formed therein for receiving a corresponding portion of a drive system component of an interchangeable surgical tool assembly that is operably attached thereto.
  • the solenoid 402 is wired to or otherwise communicates with the handle circuit board assembly 220 and the control system or CPU 224.
  • the solenoid 402 is "spring loaded" such that when the solenoid 402 is unactuated, the spring component thereof biases the third drive actuator 410 back to an unactuated starting position.
  • the reconfigurable handle assembly 20 may be advantageously employed to actuate a variety of different interchangeable surgical tool assemblies.
  • the handle assembly 20 includes a tool mounting portion that is generally designated as 500 for operably coupling an interchangeable surgical tool assembly thereto.
  • the tool mounting portion 500 includes two inwardly facing dovetail receiving slots 502 that are configured to engage corresponding portions of a tool attachment module portion of the interchangeable surgical tool assembly.
  • Each dovetail receiving slot 502 may be tapered or, stated another way, be somewhat V-shaped.
  • the dovetail receiving slots 502 are configured to releasably receive corresponding tapered attachment or lug portions that are formed on a portion of the tool attachment nozzle portion of the interchangeable surgical tool assembly.
  • Each interchangeable surgical tool assembly may also be equipped with a latching system that is configured to releasable engage corresponding retention pockets 504 that are formed in the tool mounting portion 500 of the handle assembly 20.
  • the various interchangeable surgical tool assemblies may have a "primary" rotary drive system that is configured to be operably coupled to or interface with the first rotary drive system 310 as well as a “secondary" rotary drive system that is configured to be operably coupled to or interface with the second rotary drive system 320.
  • the primary and secondary rotary drive systems may be configured to provide various rotary motions to portions of the particular type of surgical end effector that comprises a portion of the interchangeable surgical tool assembly.
  • the tool mounting portion 500 of the handle assembly 20 also includes a pair of insertion ramps 506 that are configured to bias portions of the primary and secondary rotary drive systems of the interchangeable surgical tool assembly distally during the coupling process so as to facilitate alignment and operable coupling of the primary rotary drive system to the first rotary drive system 300 on the handle assembly 20 and the secondary rotary drive system to the second rotary drive system 320 on the handle assembly 20.
  • the interchangeable surgical tool assembly may also include a "tertiary" axial drive system for applying axial motion(s) to corresponding portions of the surgical end effector of the interchangeable surgical tool assembly.
  • a "tertiary" axial drive system for applying axial motion(s) to corresponding portions of the surgical end effector of the interchangeable surgical tool assembly.
  • the third drive actuator member 410 is provided with a socket 414 that is configured to operably receive a lug or other portion of the tertiary axial drive system therein.
  • FIG. 15 An interchangeable tool assembly 2000 is illustrated in FIG. 15 .
  • the interchangeable tool assembly 2000 is similar to the interchangeable tool assembly 1000 in many respects, but is different than the interchangeable tool assembly 1000 in certain other respects.
  • the interchangeable assembly 2000 is a circular stapling assembly.
  • the circular stapling assembly 2000 comprises a shaft portion 2100 and an end effector 2200.
  • the shaft portion 2100 comprises a proximal portion which is releasably attachable to the handle assembly 20, for example.
  • the end effector 2200 comprises a first portion 2210 rotatably attached to the shaft portion 2100 about an articulation joint 2300.
  • the end effector 2200 further comprises a second portion 2220 releasably attached to the first portion 2210.
  • the second portion 2220 comprises a cartridge portion 2222 including an annular array of staple cavities 2224 defined therein and a staple stored in each staple cavity 2224.
  • the second portion 2220 further comprises an anvil 2230 including a tissue compression surface 2232 and an annular array of forming pockets or forming pockets 2234 ( FIG. 27 ) registered with the staple cavities 2224 which are configured to deform the staples when the staples are ejected from the staple cavities 2224.
  • the second portion 2220 of the end effector 2200 is selectively attachable to and selectively detachable from the first portion 2210 of the end effector 2200.
  • the second portion 2220 comprises an outer housing 2227 including a proximal connector 2229 which is configured to be received within an aperture, or chamber, 2218 defined in a housing 2217 of the first portion 2210.
  • the fit between the connector 2229 of the housing 2227 and the housing 2217 of the first portion 2210 is snug.
  • a compression fit between the connector 2229 and the housing 2217 can prevent the second portion 2220 from being accidentally displaced longitudinally and/or rotationally relative to the first portion 2210.
  • a detent member can be utilized to releasably secure the second portion 2220 to the first portion 2210 of the end effector 2200.
  • the second portion 2220 of the end effector 2200 is interchangeable with other second portions such as a second portion 2220', a second portion 2220", a second portion 2220''', and/or another second portion 2220, for example.
  • the second portions 2220', 2220", and 2220''' are similar to the second portion 2220 in many respects.
  • each second portion 2220, 2220', 2220", and 2220''' includes a central aperture 2226 defined therein. That said, the second portions 2220', 2220", and 2220''' are different than the second portion 2220 in other respects.
  • the second portion 2220' has a larger diameter than the second portion 2220.
  • the annular array of staple cavities 2224 defined in the second portion 2220' has a larger circumference than the annular array of staple cavities 2224 defined in the second portion 2220.
  • the second portion 2220" has a larger diameter than the second portion 2220' and the annular array of staple cavities 2224 defined in the second portion 2220" has a larger circumference than the annular array of staple cavities 2224 defined in the second portion 2220'.
  • the second portion 2220''' has a larger diameter than the second portion 2220" and the annular array of staple cavities 2224 defined in the second portion 2220'' has a larger circumference than the annular array of staple cavities 2224 defined in the second portion 2220".
  • the anvil 2230 is interchangeable with other anvils such as an anvil 2230', an anvil 2230", an anvil 2230"', and/or another anvil 2230, for example.
  • the anvils 2230', 2230", and 2230'' are similar to the anvil 2230 in many respects.
  • each anvil 2230, 2230', 2230", and 2230''' comprises a longitudinal shaft 2236 including connecting flanges 2238. That said, the anvils 2230', 2230", and 2230''' are different than the anvil 2230 in other respects.
  • the anvil 2230' has a larger diameter than the anvil 2230.
  • the annular array of the forming pockets 2234 defined in the anvil 2230' has a larger circumference than the annular array of forming pockets 2234 defined in the anvil 2230 such that the forming pockets 2234 remain registered with the staple cavities 2224 defined in the second portion 2220'.
  • the anvil 2230" has a larger diameter than the anvil 2230' and the annular array of forming pockets 2234 defined in the anvil 2230" has a larger circumference than the annular array of forming pockets 2234 defined in the anvil 2230' such that the forming pockets 2234 remain registered with the staple cavities 2224 defined in the second portion 2220".
  • the anvil 2230''' has a larger diameter than the anvil 2230" and the annular array of forming pockets 2234 defined in the second portion 2220''' has a larger circumference than the annular array of forming pockets 2234 defined in the anvil 2230" such that the forming pockets 2234 remain registered with the staple cavities 2224 defined in the second portion 2220"'.
  • the shaft portion 2100 comprises a proximal connector 2120 and an elongate shaft portion 2110 extending distally from the proximal connector 2120.
  • the proximal connector 2120 comprises a first input 2318 and a second input 2418.
  • the first input 2318 is operably connected to an end effector articulation system and the second input 2418 is operably connected to an end effector clamping and staple firing system.
  • the first input 2318 and the second input 2418 can be operated in any suitable order. For instance, the first input 2318 can be rotated in a first direction to articulate the end effector 2200 in a first direction and, correspondingly, rotated in a second direction to articulate the end effector 2200 in a second direction.
  • the second input 2428 can then be rotated to close the anvil 2230 and clamp tissue against the cartridge portion 2222 of the end effector 2200. As discussed in greater detail further below, the second input 2428 can then be operated to fire the staples from the staple cavities 2224 and incise tissue captured within the end effector 2200. In various alternative embodiments, the first input 2318 and the second input 2328 can be operated in any suitable order and/or at the same time.
  • the first input 2318 is mounted to a proximal end of an articulation shaft 2310 which is rotatably mounted in the shaft portion 2010.
  • the rotatable articulation shaft 2310 comprises a distal end and a worm gear 2312 mounted to the distal end.
  • the worm gear 2312 is threadably engaged with an articulation slide 2320. More specifically, the articulation slide 2320 comprises a threaded aperture 2322 defined therein and the worm gear 2312 is threadably mated with the threaded aperture 2322.
  • the worm gear 2312 pushes the articulation slide 2320 distally ( FIG. 32 ).
  • the worm gear 2312 pulls the articulation slide 2320 proximally ( FIG. 31 ).
  • the articulation slide 2320 is slidably supported by an articulation block 2112 fixedly mounted in the distal end of the elongate shaft portion 2110. The movement of the articulation slide 2320 is limited to proximal and distal movement by the articulation block 2112 by a guide slot 2315 defined in the articulation block 2112.
  • the articulation slide 2320 further comprises a longitudinal key 2326 extending therefrom which is closely received in a longitudinal keyway 2116 defined in the bottom of the guide slot 2315 which limits the relative movement between the articulation slide 2320 and the articulation block 2112 to a longitudinal path.
  • the articulation slide 2320 is coupled to an articulation link 2330.
  • the articulation slide 2320 comprises a drive pin 2324 extending therefrom which is positioned within a proximal aperture 2334 defined in the articulation link 2330.
  • the drive pin 2324 is closely received within the aperture 2334 such that the drive pin 2324 and the sidewalls of the aperture 2334 co-operate to define an axis of rotation between the articulation slide 2320 and the articulation link 2330.
  • the articulation link 2330 is also coupled to the housing 2217 of the end effector 2200.
  • the articulation link 2330 further comprises a distal aperture 2335 defined therein and the housing 2217 comprises a pin 2215 positioned in the distal aperture 2335.
  • the pin 2215 is closely received within the aperture 2335 such that the pin 2215 and the sidewalls of the aperture 2335 co-operate to define an axis of rotation between the articulation link 2330 and the housing 2217.
  • the end effector 2200 is rotatably coupled to the articulation block 2112 of the shaft 2100 about the articulation joint 2300.
  • the housing 2217 of the end effector 2200 comprises apertures 2213 defined in opposite sides thereof and the articulation block 2112 comprises projections 2113 extending from opposite sides thereof which are positioned in the apertures 2213.
  • the projections 2113 are closely received within the apertures 2213 such that the projections 2113 and the sidewalls of the apertures 2213 co-operate to define an articulation axis about which the end effector 2200 can be articulated.
  • the articulation slide 2320 drives the proximal end of the articulation link 2330 distally.
  • the articulation link 2330 rotates about the drive pin 2324 which rotates the end effector 2200 about the articulation joint 2300.
  • the articulation slide 2320 pulls the proximal end of the articulation link 2330 proximally.
  • the articulation link 2330 In response to the proximal movement of the proximal end of the articulation link 2330, the articulation link 2330 rotates about the drive pin 2324 which rotates the end effector 2200 about the articulation joint 2300.
  • the articulation link 2330 provides at least one degree of freedom between the articulation slide 2320 and the housing 2217. As a result, the articulation link 2330 permits the end effector 2200 to be articulated through a wide range of articulation angles.
  • the proximal connector 2120 ofthe interchangeable tool assembly 2000 comprises a second input 2418.
  • the second input 2418 comprises a drive gear 2417 which is meshingly engaged with a drive gear 2416 mounted on a proximal end of a drive shaft 2410.
  • the drive shaft 2410 extends through the shaft portion 2110 and an aperture 2114 defined in the articulation block 2112, as illustrated in FIG. 19 .
  • the aperture 2114 comprises a bearing and rotatably supports the drive shaft 2410.
  • the aperture 2114 can comprise a clearance aperture. In either event, referring primarily to FIG.
  • the drive shaft 2410 extends through the articulation joint 2300 and into the chamber 2218 defined in the end effector housing 2217.
  • the drive shaft 2410 is rotatably supported by a bearing 2414 mounted to the drive shaft 2410 which is captured within a recess 2214 defined in the housing 2217 of the end effector 2200.
  • the drive shaft 2410 further comprises an output gear 2412 mounted to the distal end thereof such that the rotation of the drive shaft 2410 is transmitted to the output gear 2412.
  • the output gear 2412 of the drive shaft 2410 is operably engaged with a transmission 2420.
  • the transmission 2420 is configured to shift the end effector 2200 between a first operating mode in which the drive shaft 2410 moves the anvil 2230 relative to the cartridge body 2222 and a second operating mode in which the drive shaft 2410 fires the staples from the staple cavities 2224 and incises the tissue captured between the anvil 2230 and the cartridge body 2222.
  • the transmission 2420 comprises an orbit drive comprising a planetary plate 2421 and four planetary gears 2424 rotatably mounted to the planetary plate 2421.
  • the planetary plate 2421 comprises a clearance aperture extending through the center thereof and the drive shaft 2410 extends through the clearance aperture.
  • the planetary plate 2421 and the planetary gears 2424 are positioned in a chamber 2219 defined in the end effector housing 2217.
  • Each planetary gear 2424 is rotatable about a gear pin 2423 extending from the planetary plate 2421.
  • the gear pins 2423 are positioned along a circumference surrounding the clearance aperture.
  • the output gear 2412 is meshingly engaged with the planetary gears 2424 and, as described in greater detail below, the drive shaft 2410 drives the planetary gears 2424.
  • the drive shaft 2410 extends trough the articulation joint 2300.
  • the drive shaft 2410 is flexible.
  • the drive shaft 2410 is comprised of plastic, for example.
  • the transmission 2420 comprises a first operating mode and a second operating mode.
  • the interchangeable tool assembly 2000 further comprises a shifter 2600 movable between a first position and a second position to switch the transmission 2420 between its first operating mode and its second operating mode.
  • the shifter 2600 is in its first position, as illustrated in FIGS. 28-30 , the shifter 2600 is not engaged with the planetary plate 2421 of the transmission 2420 and, as a result, the planetary plate 2421 and the planetary gears 2424 are rotated by the drive shaft 2410.
  • the drive shaft 2410 rotates the planetary gears 2424 about their respective gear pins 2423 and the planetary gears 2424 rotate the planetary plate 2421 owing to reactionary forces between the planetary gears 2424 and an annular ring of teeth 2534 which extends around the planetary gears 2424, as described in greater detail further below.
  • the planetary plate 2421 is operably coupled with an output coupling 2430 such that the rotation of the planetary plate 2421 is transmitted to the output coupling 2430. Referring primarily to FIG.
  • the output coupling 2430 comprises an array of apertures 2433 extending around the outer perimeter thereof wherein the gear pins 2423 extending from the planetary plate 2421 extend into, and are closely received by, the apertures 2433 defined in the output coupling 2430 such that there is little, if any, relative movement between the planetary plate 2421 and the output coupling 2430.
  • the output coupling 2430 comprises a drive socket 2432.
  • the drive socket 2432 comprises a substantially hexagonal aperture, for example; however, any suitable configuration could be utilized.
  • the drive socket 2432 is configured to receive a closure shaft 2440 extending through the second portion 2220 of the end effector 2200.
  • the closure shaft 2440 comprises a proximal drive end 2442 which has a substantially-hexagonal shape that is closely received within the drive socket 2432 such that the rotation of the drive shaft 2410 is transferrable to the closure shaft 2440.
  • the closure shaft 2440 is rotatably supported within the housing 2227 of the second portion 2220 by a bearing 2444.
  • the bearing 2444 comprises a thrust bearing, for example; however, the bearing 2444 may comprise any suitable bearing.
  • the closure shaft 2440 comprises a threaded portion 2446 that is threadably engaged with a threaded aperture 2456 defined in a trocar 2450.
  • the anvil 2230 is attachable to the trocar 2450 which can be translated to move the anvil 2230 toward and/or away from the cartridge body 2222.
  • the trocar 2450 comprises at least one longitudinal key slot 2459 defined therein which is configured to co-operate with at least one longitudinal key extending from an inner surface 2546 of the drive sleeve 2540.
  • the drive sleeve 2540 is part of the staple firing system, discussed further below, and the reader should understand that the trocar 2450 and the drive sleeve 2540, one, slide relative to one another, and, two, co-operatively inhibit relative rotational movement therebetween.
  • the closure shaft 2440 can displace, or translate, the trocar 2450 distally when the closure shaft 2440 is rotated in a first direction and, correspondingly, displace, or translate, the trocar 2450 proximally when the closure shaft 2440 is rotated in a second, or opposite, direction.
  • the anvil 2230 is attachable to the trocar 2450.
  • the anvil 2230 comprises connecting flanges 2238 which are configured to engage and grip the trocar 2450.
  • the connecting flanges 2238 comprise cantilever beams which are connected to the shaft portion 2236 of the anvil 2230.
  • the trocar 2450 comprises retention notches, or recesses, 2458 which are configured to releasably receive the connecting flanges 2238 when the anvil 2230 is assembled to the trocar 2450.
  • the retention notches 2458 and the connecting flanges 2238 are configured to resist the inadvertent detachment of the anvil 2230 from the trocar 2450.
  • the connecting flanges 2238 are separated by longitudinal slots 2237.
  • the longitudinal slots 2237 are configured to receive longitudinal ribs 2457 extending from the trocar 2450 when the anvil 2230 is assembled to the trocar 2450.
  • the ribs 2457 are closely received within the slots 2237 and, as a result, the anvil 2230 is inhibited from rotating relative to the trocar 2450.
  • the shifter 2600 comprises an electrically-actuated motor, for example, which is utilized to shift the transmission 2420 of the end effector 2200.
  • the shifter 2600 can comprise any suitable device which is electrically and/or manually actuated.
  • the shifter 2600 is in signal communication with a processor of the surgical stapling instrument and in power communication with a battery of the surgical stapling instrument.
  • insulated electrical wires for example, extend between the shifter 2600 and a handle of the surgical instrument such that the processor can communicate with the shifter 2600 and the battery can supply power to the shifter 2600.
  • the shifter 2600 can comprise a wireless signal receiver and the processor can communicate wirelessly with the shifter 2600.
  • power can be supplied wirelessly to the shifter 2600, such as through an inductive circuit, for example.
  • the shifter 2600 can comprise its own power source.
  • the shifter 2600 comprises a housing mounted in the chamber 2218 defined in the proximal end of the end effector 2200.
  • the shifter 2600 comprises a clutch key, or toggle, 2602 and an output shaft 2604 movable between a first position and a second position relative to the shifter housing.
  • the clutch key 2602 comprises a first lock tooth 2608 and a second lock tooth 2609 and, when the clutch key 2602 is in its first position, the first lock tooth 2608 is engaged with a firing tube 2530 of the staple firing system and, concurrently, the second lock tooth 2609 is disengaged from the planetary plate 2421 of the transmission 2420.
  • the first lock tooth 2608 is positioned in an aperture 2538, which is part of an annular array of apertures 2538 defined around the firing tube 2530, and the second lock tooth 2609 is not positioned in an aperture 2429, which is part of an annular array of apertures 2429 defined around the planetary plate 2421.
  • the shifter 2600 prevents the firing tube 2530 from rotating and, accordingly, locks out the staple firing system when the clutch key 2602 is in its first position.
  • the staple firing system has been locked out by the shifter 2600 when the clutch key 2602 is in its first position, the drive shaft 2410 can rotate the planetary plate 2421 and operate the anvil closure system, as discussed above.
  • the firing tube 2530 comprises an inner annular rack of teeth 2534 defined in an inner sidewall 2532 thereof.
  • the planetary gears 2424 are operably intermeshed with the rack of teeth 2534.
  • the shifter 2600 is in its first position, as illustrated in FIG. 28 , the firing tube 2530 is held in position by the shifter 2600 and the planetary gears 2424 are rotatable relative to the firing tube 2530 and the rack of teeth 2534 by the drive shaft 2410.
  • the planetary gears 2424 are rotated about a longitudinal drive axis defined by the drive shaft 2410 and, at the same time, rotated about axes defined by their respective gear pins 2423.
  • the planetary gears 2424 are directly driven by the drive shaft 2410 and, owing to reactionary forces created between the planetary gears 2424 and the firing tube 2530, the planetary gears 2424 drive and rotate the planetary plate 2421.
  • the shifter 2600 is actuated to move the clutch key 2602 into its second position, the first lock tooth 2608 is disengaged from the firing tube 2530 and, concurrently, the second lock tooth 2609 is engaged with the planetary plate 2421.
  • the planetary plate 2421 is held in position by the shifter 2600 when the clutch key 2602 is in its second position and, as a result, the closure drive has been locked out and cannot be operated to move the anvil 2230.
  • the output gear 2412 drives and rotates the planetary gears 2424 relative to the planetary plate 2421 about their respective gear pins 2423.
  • the planetary gears 2424 drive the firing tube 2530 via the rack of teeth 2534 and rotate the firing tube 2530 about its longitudinal axis.
  • the firing tube 2530 is operably coupled with the drive sleeve 2540 of the staple firing system. More specifically, the inner sidewall 2532 of the firing tube 2530 comprises longitudinal slots 2535 defined therein which are configured to closely receive longitudinal ribs 2545 defined on the drive sleeve 2540 such that the drive sleeve 2540 rotates with the firing tube 2530.
  • the drive sleeve 2540 further comprises a threaded distal end 2542 which is threadably engaged with a drive collar 2550. More specifically, the drive collar 2550 comprises a threaded aperture 2552 which is threadably engaged with the threaded distal end 2542.
  • the drive collar 2550 is positioned in an aperture 2228 defined in the housing of the end effector 2200 and is prevented from rotating within the aperture 2228 by a longitudinal rib and groove arrangement, for example.
  • the rotation of the drive sleeve 2540 translates the drive collar 2550 longitudinally.
  • the drive collar 2550 is advanced distally if the drive sleeve 2540 is rotated in a first direction and retracted proximally if the drive sleeve 2540 is rotated in a second, or opposite, direction.
  • the drive collar 2550 pushes a staple driver block 2560 and a cutting member 2570, such as a knife, for example, distally during a firing stroke of the staple firing system. More specifically, the drive collar 2550 pushes the staple driver block 2560 and the cutting member 2570 between a proximal, unfired position in which the staples are positioned in the staple cavities 2224 defined in the cartridge body portion 2222 and the cutting member 2570 is recessed below the deck surface of the cartridge body portion 2222 and a distal, fired position in which the staples have been deformed against the anvil 2230 and the tissue captured between the anvil 2230 and the cartridge body portion 2222 has been transected by the cutting member 2570.
  • a proximal, unfired position in which the staples are positioned in the staple cavities 2224 defined in the cartridge body portion 2222 and the cutting member 2570 is recessed below the deck surface of the cartridge body portion 2222 and a distal, fired position in which the staples have been deformed against the anvil 2230 and the
  • the drive collar 2550 comprises a drive recess 2554 which is configured to abut the staple driver block 2560 and the cutting member 2570 as the drive collar 2550 is advanced distally.
  • the staple driver block 2560 comprises a plurality of staple cradles defined therein wherein each staple cradle is configured to support the base of a staple.
  • the staple cradles are aligned with the staple cavities 2224 defined in the cartridge body portion 2222 and are arranged in at least two concentric rows.
  • the staple driver block 2560 and the cutting member 2570 are attached to the drive collar 2550 such that, when the drive collar 2550 is moved proximally away from the anvil 2230, the staple driver block 2560 and the cutting member 2570 are pulled proximally by the drive collar 2550.
  • the staple driver block 2560 and the cutting member 2570 comprise one or more hooks which extend into apertures 2557 defined in the drive collar 2550.
  • the staple driver block 2560 and the cutting member 2570 can be retracted such that they are completely retracted below the deck surface of the cartridge body portion 2222.
  • the end effector 2200 is operable in a third operating mode in which the drive shaft 2410 moves the anvil 2230, the staple driver block 2560, and the cutting member 2570 relative to the cartridge body 2222 at the same time.
  • each second portion comprises a housing connector 2229 which engages the housing 2217 of the first portion 2210 when the second portion is assembled to the first portion 2210.
  • each second portion comprises a closure shaft 2440 which operably engages the drive socket 2432 of the first portion 2210 when the second portion is assembled to the first portion 2210.
  • each second portion comprises a drive sleeve 2540 which operably engages the firing tube 2530 of the first portion 2210 when the second portion is assembled to the first portion 2210.
  • a tool assembly 2000' is interchangeable with the tool assembly 2000.
  • the tool assembly 2000' is similar to the tool assembly 2000 in many respects; however, the tool assembly 2000' is configured to apply circular staple lines having larger diameters than the circular staple lines applied by the tool assembly 2000.
  • the tool assembly 2000' comprises, among other things, a wider second portion 2220', staple driver 2560', knife assembly 2570', cartridge body 2222', and anvil 2230'.
  • a tool assembly 2000" is interchangeable with the tool assembly 2000.
  • the tool assembly 2000 is similar to the tool assemblies 2000 and 2000' in many respects; however, the tool assembly 2000” is configured to apply circular staple lines having larger diameters than the circular staple lines applied by the tool assembly 2000'.
  • the tool assembly 2000 comprises, among other things, a wider second portion 2220", staple driver 2560", knife assembly 2570", cartridge body 2222", and anvil 2230".
  • a tool assembly 2000''' is interchangeable with the tool assembly 2000.
  • the tool assembly 2000''' is similar to the tool assemblies 2000, 2000', and 2000" in many respects; however, the tool assembly 2000''' is configured to apply circular staple lines having larger diameters than the circular staple lines applied by the tool assembly 2000".
  • the tool assembly 2000''' comprises, among other things, a wider second portion 2220"', staple driver 2560''', knife assembly 2570''', cartridge body 2222''', and anvil 2230'''.
  • a surgical instrument can have any suitable number of operating modes.
  • a surgical stapling instrument comprises a transmission which includes a first operating mode which fires the staples, a second operating mode which deploys the cutting member, and a third operating mode which both fires the staples and deploys the cutting member at the same time.
  • the first operating mode the cutting member is not deployed.
  • the processor of such a surgical instrument can be programmed such that the instrument cannot be placed in the second operating mode without having first completed the first operating mode.
  • the user of the surgical instrument can decide whether or not to cut the tissue after the staples have been fired.
  • a cartridge body 2222' comprises an annular outer row of staple cavities 2224 and an annular inner row of staple cavities 2224'.
  • the staple cavities 2224 are defined in a first step of the cartridge body deck and the staple cavities 2224' are defined in a second step of the cartridge body deck.
  • the second step extends above the first step. Stated another way, the first step has a first deck height and the second step has a second deck height which is taller than the first deck height.
  • a deck wall separates the first step and the second step. In various embodiments, the deck wall is sloped. In certain embodiments, the deck wall is orthogonal to the first step and/or the second step.
  • the cartridge body 2222' further comprises cavity extensions 2229' extending from the first step of the deck.
  • the cavity extensions 2229' surround the ends of the staple cavities 2224 and extend the staple cavities 2224 above the first step.
  • the cavity extensions 2229' can at least partially control the staples above the first step as the staples are ejected from the staple cavities 2224.
  • the cavity extensions 2229' are also configured to contact and compress tissue captured against the cartridge body 2222'.
  • the cavity extensions 2229' can also control the flow of tissue relative to the cartridge body 2222'.
  • the cavity extensions 2229' can limit the radial flow of the tissue.
  • the cavity extensions 2229' can have any suitable configuration and can extend any suitable height from the first step. In at least one instance, the top surfaces of the cavity extensions 2229' are aligned with, or have the same height as, the second step, for example. In other instances, the cavity extensions 2229' can extend above or below the second step.
  • the staple cavities 2224 each comprise a first staple positioned therein having a first unformed height.
  • the staple cavities 2224' each comprise a second staple positioned therein having a second unformed height which is different than the first unformed height.
  • the first unformed height is taller than the second unformed height; however, the second unformed height could be taller than the first unformed height.
  • the first unformed staple height and the second unformed staple height is the same.
  • the first staples are deformed to a first deformed height and the second staples are deformed to a second deformed height which is different than the first deformed height.
  • the first deformed height is taller than the second deformed height.
  • the second deformed height could be taller than the first deformed height.
  • Such an arrangement could improve the pliability of the tissue along the inner transection line.
  • the first deformed height and the second deformed height is the same.
  • an interchangeable tool assembly can comprise, among other things, a shaft, an end effector, and a replaceable staple cartridge.
  • the replaceable staple cartridge comprises a closure drive configured to move open and close the end effector to capture tissue within the end effector and a firing drive configured to staple and cut the tissue captured within the end effector.
  • the closure drive and the firing drive of the end effector are operably coupled with a corresponding closure drive and firing drive of the shaft when the replaceable staple cartridge is assembled to the shaft.
  • the replaceable staple cartridge and/or the shaft can comprise a lockout which prevents the replaceable staple cartridge from being operated unless the replaceable staple cartridge is properly attached to the shaft.
  • an interchangeable tool assembly 3000 comprises a shaft 3010 and a replaceable staple cartridge 3020. Similar to the above, the replaceable staple cartridge 3020 comprises a closure drive input and a firing drive input which are operably coupled with a closure drive output and a firing drive output, respectively, when the staple cartridge 3020 is fully seated onto the shaft 3010. The operation of such closure and firing systems are not repeated herein for the sake of brevity.
  • the interchangeable tool assembly 3000 further comprises a lockout circuit 3090.
  • the lockout circuit 3090 includes conductors 3096 and contacts 3092.
  • a first contact 3092 is electrically coupled to a first conductor 3096 and a second contact 3092 is electrically coupled to a second conductor 3096.
  • the first contact 3092 is not electrically coupled to the second contact 3092 prior to the staple cartridge 3020 being fully seated onto the shaft 3010.
  • the staple cartridge 3020 comprises a contact bridge 3094 which engages and electrically couples the contacts 3092 when the staple cartridge 3020 is fully seated onto the shaft 3010.
  • the contacts 3092 and the contact bridge 3094 are configured and arranged such that the contact bridge 3094 does not electrically couple the contacts 3092 when the staple cartridge 3020 is only partially seated onto the shaft 3010.
  • the interchangeable tool assembly 3000 is usable with a surgical instrument system which includes a manually-operable handle and/or a robotic system, for example.
  • the surgical instrument system includes an electric motor configured to drive the staple firing system of the tool assembly 3000 and, in addition, a controller configured to operate the electric motor.
  • the lockout circuit of the tool assembly 3000 is in communication with the controller. When the controller detects that the contact bridge 3094 is not engaged with the contacts 3092, or that the lockout circuit is in an open condition, the controller prevents the electric motor from operating the staple firing system. In various instances, the controller is configured such that it does not supply power to the electric motor when the lockout circuit is in an open condition.
  • the controller is configured to supply power to the electric motor such that it can operate the closure system but not the firing system when the lockout circuit is in an open condition.
  • the controller operates a transmission coupled to the electric motor such that the output of the electric motor is only directed to the closure system.
  • the controller detects that the contact bridge 3094 is engaged with the contacts 3092, or that the lockout circuit is in a closed condition, the controller allows the electric motor to operate the staple firing system.
  • a surgical instrument system comprises a handle
  • the controller can actuate a trigger lock which prevents a firing trigger of the handle from being actuated when the controller detects that the lockout circuit is in an open configuration.
  • the controller can retract the trigger lock and allow the firing trigger to be actuated.
  • a non-motorized firing drive can be driven by a handcrank, for example.
  • an anvil 2230 can be assembled to the trocar shaft 2450 of the closure drive of the tool assembly 2000.
  • the connecting flanges 2238 of the anvil 2230 are configured to engage a recess 2458 defined in the trocar shaft 2450 to connect the anvil 2230 thereto.
  • the mis-assembly of the anvil 2230 to the trocar shaft 2450 can frequently occur when the trocar shaft 2450 is not sufficiently extended above the deck of the staple cartridge 2222 when a clinician attempts to assemble the anvil 2230 to the trocar shaft 2450.
  • the anvil 2230 is sufficiently attached to the trocar shaft 2450 such that the trocar shaft 2450 can move the anvil 2230 toward the staple cartridge 2222 but, when the anvil 2230 begins to compress the tissue against the staple cartridge 2222, the anvil 2230 can detach from the trocar shaft 2450.
  • the tool assembly 2000 comprises a cartridge body 3120 comprising a deck 3121 configured to support tissue when the tissue is compressed against the cartridge body 3120 by the anvil 2130.
  • the tool assembly 3100 further comprises a closure drive configured to move the anvil 2130 relative to the cartridge body 3120.
  • the closure drive comprises a trocar shaft 3150 which, similar to the above, includes a recess defined therein.
  • the recess comprises a distal shoulder 3158 which is configured to retain the anvil 2130 to the trocar shaft 3150.
  • the tool assembly 3100 further comprises a firing drive configured to eject staples from the cartridge body 3120.
  • the firing drive comprises a rotatable shaft 3162 and a translatable collar 3160 threadably engaged with the rotatable shaft 3162 which is configured to eject staples from the cartridge body 3120.
  • the rotatable shaft 3162 comprises a longitudinal aperture 3164 defined therein and the trocar shaft 3150 extends through the aperture 3164.
  • the closure drive further comprises a clip 3190 mounted to the trocar shaft 3150.
  • the clip 3190 comprises a base 3192 mounted within a slot defined in the trocar shaft 3150.
  • the clip 3190 further comprises compliant arms, or appendages, 3198 extending from the base 3192.
  • the arms 3198 are movable between an extended position ( FIG. 39 ) and a deflected position ( FIG. 40 ). When the arms 3198 are in their deflected position, as illustrated in FIG. 40 , the anvil 2130 can be locked to the trocar shaft 3150.
  • the arms 3198 are held in their deflected position by the translatable collar 3160 of the firing drive when the trocar shaft 3150 has been sufficiently extended above the deck 3121 of the cartridge body 3120, as illustrated in FIG. 40 .
  • the translatable collar 3160 comprises an annular shoulder 3168 configured to resiliently bias the arms 3198 inwardly when the arms 3198 are brought into contact with the shoulder 3168.
  • the arms 3198 When the trocar shaft 3150 is not in a sufficiently extended position above the cartridge deck 3121, the arms 3198 are not biased inwardly by the shoulder 3168. In such instances, the arms 3198 are in their extended position, as illustrated in FIG. 39 . When the arms 3198 are in their extended position, the arms 3198 prevent the anvil 2130 from being attached to the trocar shaft 3150. More specifically, the arms 3198 prevent the connecting flanges 2138 of the anvil 2130 from being seated behind the shoulder 3158 defined in the trocar shaft 3150.
  • the arms 3198 prevent the anvil 2130 from being partially attached to the trocar shaft 3150 and, as a result, the clinician attempting to assemble the anvil 2130 to the trocar shaft 3150 cannot partially assemble the anvil 2130 to the trocar shaft 3150 and can avoid the issues discussed above.
  • the anvil 2130 is often assembled to the trocar shaft 3150 in situ, or within a patient, and the proper assembly of the anvil 2130 to the trocar shaft 3150 expedites the completion of the surgical technique being used.
  • the system discussed above provides a lockout which prevents a partially assembled anvil from being compressed against the tissue.
  • an interchangeable tool assembly 3200 comprises a lockout configured to prevent a closure drive from being retracted without an anvil attached thereto, as discussed in greater detail below.
  • the tool assembly 3200 comprises a shaft 3210 and an end effector 3220.
  • the end effector 3220 includes an outer housing 3227, a cartridge body 3222, and a longitudinal aperture 3226 defined therethrough.
  • the tool assembly 3200 further comprises a closure drive including a trocar shaft 3250 and an anvil 3230 attachable to the trocar shaft 3250. Similar to the above, the closure drive is configured to move the anvil 3230 toward and away from the cartridge body 3222.
  • the trocar shaft 3250 is movable between an extended position and a retracted position.
  • FIGS. 42 and 43 both illustrate the trocar shaft 3250 in its extended position.
  • the tool assembly 3200 further comprises a retraction lock 3290 configured to prevent the trocar shaft 3250 from being moved from its extended position ( FIGS. 42 and 43 ) toward its retracted position when the anvil 3230 is not assembled to the trocar shaft 3250.
  • the retraction lock 3290 comprises a lock arm 3292 rotatably mounted to the housing 3227 about a projection, or pin, 3294.
  • the retraction lock 3290 further comprises a spring 3296 engaged with the lock arm 3292 which is configured to bias the lock arm 3292 toward the trocar shaft 3250.
  • the trocar shaft 3250 comprises a lock shoulder 3258 and, when the anvil 3230 is not assembled to the trocar shaft 3250 as illustrated in FIG.
  • the lock arm 3292 is configured to catch the lock shoulder 3258 and prevent the trocar shaft 3250 from being moved proximally. More specifically, the lock arm 3292 comprises a catch 3298 configured to slide under the lock shoulder 3258.
  • the anvil 3230 When the anvil 3230 is assembled to the trocar shaft 3250, as illustrated in FIG. 43 , the anvil 3230 contacts the lock arm 3292 and displaces the lock arm 3292 away from the lock shoulder 3258. At such point, the trocar shaft 3250 has been unlocked and can be moved toward the cartridge body 3222 into its retracted position.
  • an interchangeable tool assembly 3300 comprises a closure drive, a staple firing drive, and a lockout configured to prevent the staple firing drive from being operated until the anvil of the closure drive has been set to a proper tissue gap, as discussed in greater detail below.
  • the tool assembly 3300 comprises a shaft 3310 and an end effector 3320.
  • the end effector 3320 includes an inner frame 3329, an outer housing 3327, and a cartridge body 3322.
  • the closure drive includes a trocar shaft 3350 and an anvil 2230 attachable to the trocar shaft 3350.
  • the trocar shaft 3350 is movable between an extended position ( FIG. 45 ) and a retracted position ( FIG. 46 ) to move the anvil 2230 toward and away from the cartridge body 3322.
  • the firing drive includes a rotatable shaft 3360 which is configured to displace a firing drive distally to eject the staples stored in the cartridge body 3322.
  • the end effector 3320 comprises a firing drive lock 3390 movably mounted to the inner frame 3329.
  • the firing drive lock 3390 comprises a lock pin 3394 and a lock spring 3398 positioned around the lock pin 3394.
  • the lock pin 3394 comprises a head 3392 and a stop 3396.
  • the lock spring 3398 is positioned intermediate the stop 3396 and a sidewall of a cavity 3328 defined in the inner frame 3329.
  • the lock spring 3398 biases the lock pin 3394 into a lock aperture 3364 defined in the rotatable shaft 3360 of the staple firing drive.
  • the interaction between the lock pin 3394 and the sidewalls of the lock aperture 3364 prevent the shaft 3360 from being rotated to fire the staples from the cartridge body 3322.
  • the trocar shaft 3350 engages the head 3392 of the lock pin 3394.
  • the head 3392 comprises a cam surface defined thereon which is configured to be engaged by the trocar shaft 3350 to move the firing drive lock 3390 between a locked configuration ( FIG. 45 ) and an unlocked configuration ( FIG. 46 ).
  • the drive lock 3390 is in its unlocked configuration, the shaft 3360 of the firing drive can be rotated.
  • the firing drive lockout of the tool assembly 3300 requires the anvil 2230 to be moved into a predetermined position, or within a range of predetermined positions, before the staples can be fired. Moreover, the firing drive lockout of the tool assembly 3300 requires the tissue gap between the anvil 2230 and the cartridge body 3322 to be less than a certain distance before the staples can be fired. As a result, the position of the anvil 2230 and/or the closure system deactivates the staple firing lockout. Such an arrangement can assist in preventing the malformation of the staples and/or the undercompression of the tissue, among other things.
  • an interchangeable tool assembly 3400 comprises a closure drive configured to clamp tissue, a staple firing drive, and a firing drive lockout 3490 configured to prevent the staple firing drive from being operated prior to the closure drive applying a sufficient clamping pressure to the tissue.
  • the closure drive comprises a trocar shaft 3450 and an anvil, such as anvil 2230, for example, attached to the trocar shaft 3450. Similar to the above, the trocar shaft 3450 is movable from an extended position ( FIG. 48 ) to a retracted position ( FIG. 49 ) to compress tissue against a cartridge body of the tool assembly 3400.
  • the firing drive comprises a rotatable shaft 3460 configured to displace a staple driver distally and eject staples from the cartridge body.
  • the firing drive lockout 3490 is positioned intermediate the trocar shaft 3450 of the closure drive and the rotatable shaft 3460 of the firing drive.
  • the firing drive lockout 3490 comprises a distal plate 3492, a proximal plate 3494, and a spring 3493 positioned intermediate the distal plate 3492 and the proximal plate 3494.
  • the firing drive lockout 3490 further comprises a lock pin 3498 movable between a locked configuration ( FIG. 48 ) in which the lock pin 3498 is engaged with the shaft 3460 and an unlocked configuration ( FIG. 49 ) in which the lock pin 3498 is disengaged from the shaft 3460.
  • the lock pin 3498 is positioned in a pin chamber 3496 defined between the distal plate 3492 and the proximal plate 3494.
  • the lock pin 3498 comprises a beveled head positioned intermediate a cam 3495 defined on the distal plate 3492 and a cam 3495 defined on the proximal plate 3494.
  • the trocar shaft 3450 pushes the distal plate 3492 proximally and the cam 3495 defined on the distal plate 3492 engages the head of the lock pin 3498.
  • the cam 3495 defined on the distal plate 3492 in co-operation with the cam 3495 defined on the proximal plate 3494, displace the lock pin 3498 into its unlocked configuration, as illustrated in FIG. 49 .
  • the cams 3495 of the firing drive lockout 3490 squeeze the head of the lock pin 3498 as the distal plate 3492 is moved toward the proximal plate 3494 by the trocar shaft 3450. More specifically, the cams 3495 drive the lock pin 3498 inwardly and out of engagement with the rotatable shaft 3460.
  • the lock pin 3498 is positioned in a lock aperture 3468 defined in the shaft 3460 when the lock pin 3498 is in its locked configuration and, owing to the interaction between the lock pin 3498 and the sidewalls of the lock aperture 3468, the lock pin 3498 prevents the shaft 3460 from rotating. As a result, the staples cannot be fired from the cartridge body by the firing drive.
  • the shaft 3460 can include a circumferential array of lock apertures 3468 defined in the shaft 3460, each of which is configured to receive the lock pin 3498 and lockout the firing drive.
  • the firing drive lockout 3490 further comprises a biasing member, such as a spring 3499, for example, which is configured to bias the lock pin 3498 into a lock aperture 3468.
  • the spring 3493 of the firing drive lockout 3490 is configured to resist the proximal movement of the trocar shaft 3450.
  • the spring 3493 is a linear coil spring; however, any suitable spring could be used. Moreover, more than one spring could be used.
  • the spring 3493, or spring system has a stiffness which applies a spring force to the distal plate 3492 ofthe firing drive lockout 3490 as the trocar shaft 3450 is retracted. Stated another way, the force applied to the distal plate 3492 by the spring 3493 increases in proportion to the distance in which the trocar shaft 3450 is displaced proximally. The spring force generated by the spring 3493 opposes the clamping force that the anvil 2230 is applying to the tissue.
  • the clamping force must overcome a certain, or predetermined, spring force being generated by the spring 3493 in order to sufficiently displace the distal plate 3492 and unlock the firing drive.
  • the tissue clamping force must meet a predetermined threshold before the firing drive lockout 3490 can be deactivated and the staple firing drive can be actuated.
  • a staple firing drive drives staples against an anvil to deform the staples to a desired formed height.
  • the staple firing drive is also configured to push a cutting member, such as a knife, for example, distally to cut tissue captured between the cartridge body and the anvil.
  • a cutting member such as a knife
  • the knife is exposed above the deck of the cartridge body. That said, the anvil is positioned in close relationship to the cartridge body when the anvil is in its closed, or clamped, position and the knife is, for the most part, covered by the anvil even though the knife is exposed above the cartridge body.
  • FIGS. 52-54 which comprises a lockout 3590 configured to prevent the anvil from being moved into its open position while the knife is exposed above the cartridge deck.
  • the tool assembly 3500 comprises a closure drive and a firing drive.
  • the closure drive comprises a trocar shaft 3550 and an anvil 3530 releasably attachable to the trocar shaft 3550. Similar to the above, the trocar shaft 3550 is translatable proximally and distally by a rotatable closure shaft 2440 threadably engaged with the trocar shaft 3550.
  • the firing drive comprises a rotatable shaft 3562 and a translatable collar 3560 threadably engaged with the rotatable shaft 3562. Similar to the above, the collar 3560 is translatable proximally and distally when the shaft 3562 is rotated in first and second directions, respectively. Also similar to the above, the collar 3560 of the firing drive is configured to advance and retract an array of staple drivers and a knife assembly 2570 toward and away from the anvil 3530.
  • the lockout 3590 comprises a lock arm 3592 rotatably mounted to the shaft 3562 of the firing drive about a pivot 3594.
  • the lockout 3590 further comprises a biasing member, or spring, 3599 engaged with the lock arm 3592 which is configured to bias the lock arm 3592 into contact with the anvil 3530.
  • the anvil 3530 is assembled to the trocar shaft 3550 and the trocar shaft 3550 is then retracted to position the anvil 3530 in its closed, or clamped, position relative to the cartridge body.
  • the lock arm 3592 ofthe lockout 3590 slides against the outer surface of the anvil 3530 until the lock arm 3592 is aligned with a lock recess 3532 defined in the anvil 3530. At such point, the spring 3599 biases the lock arm 3592 into the lock recess 3532, as illustrated in FIG. 53 . More specifically, the lock arm 3592 is positioned behind a lock shoulder which defines the lock recess 3532.
  • the firing drive can then be operated to fire the staples and cut the tissue. In such instances, the cutting edge of the knife assembly 2570 is exposed above the cartridge body and, owing to the lockout 3590, the closure drive is locked out, or prevented from being opened, until the cutting edge of the knife assembly 2570 is no longer exposed.
  • the lock arm 3592 further comprises a reset tab 3593 extending therefrom.
  • the collar 3560 of the firing drive further comprises a cam 3563 configured to engage the reset tab 3593 when the collar 3560 and the knife assembly 2570 are retracted proximally by the firing drive.
  • the cam 3563 is configured to rotate the lock arm 3592 downwardly out of engagement with the lock shoulder defined in the lock recess 3532 and unlock the closure drive.
  • the cam 3563 is configured to unlock the closure drive when the cutting edge of the knife assembly 2570 has been retracted below the cartridge deck; however, in other embodiments, the cam 3563 can unlock the closure drive when the cutting edge is flush with, or at least substantially flush with, the cartridge deck.
  • the closure drive may not be unlocked until the knife assembly 2570 has been completely retracted. Once the closure drive has been unlocked, the closure drive can be operated to move the anvil 3530 to an open, or unclamped, position once again.
  • a tool assembly can include a lockout configured to prevent the tool assembly from being re-clamped onto tissue after it has been used to staple tissue.
  • an interchangeable tool assembly 3600 comprises a closure drive configured to position an anvil, such as anvil 2230, for example, relative to a staple cartridge and a firing drive configured to drive staples from the staple cartridge.
  • anvil 2230 is attachable to a translatable trocar shaft 3650 of the closure drive.
  • the firing drive comprises a rotatable shaft 3660, a translatable collar 2550 threadably engaged with the rotatable shaft 3660, and a staple firing driver 2560 displaceable by the rotatable shaft 3660.
  • the closure drive is operable to position the anvil 2230 in a clamped position relative to the staple cartridge and the firing driver is then operable to fire the staples into tissue captured between the anvil 2230 and the staple cartridge. Thereafter, the closure drive is operated to open the anvil 2230 and release the tissue.
  • the tool assembly 3600 comprises a lockout 3690 configured to prevent the anvil 2230 from being reclamped onto the tissue.
  • the lockout 3690 comprises a lock arm 3692 rotatably mounted to the rotatable shaft 3660 which is held in an unlocked configuration by the firing drive as the closure drive moves the anvil 2230 between an open, unclamped position ( FIG. 53 ) and a closed, clamped position ( FIG. 54 ).
  • the lock arm 3692 is held in its unlocked configuration between the rotatable shaft 3660 and the translatable collar 2550 as the trocar shaft 3650 and the anvil 2230 are moved relative to the firing drive to position the anvil 2230 relative to the staple cartridge.
  • the arm 3692 is held in its unlocked configuration until the firing drive is operated, as illustrated in FIG. 55 .
  • the shaft 3460 is rotated in a first direction, the collar 2550 is displaced distally and a spring 3699 of the lockout 3690 can bias the lock arm 3692 against the trocar shaft 3650.
  • the trocar shaft 3650 rotates relative to the lock arm 3692 as the collar 2550 is displaced distally to fire the staples and then retracted proximally.
  • the closure drive can then be operated to re-open the anvil 2230 to unclamp the tissue and/or detach the anvil 2230 from the trocar shaft 3650.
  • the spring 3699 biases the lock arm 3692 into a lock recess 3652 defined in the trocar shaft 3650 and/or anvil 2230.
  • the lock arm 3692 prevents the trocar shaft 3650 from being retracted proximally.
  • the lock arm 3692 will abut a lock shoulder defined in the lock recess 3652 and prevent the retraction of the trocar shaft 3650 and anvil 2230.
  • the lockout 3690 prevents the anvil 2230 from being re-clamped onto tissue after the tool assembly 3600 has undergone, or at least partially undergone, a firing cycle and the tool assembly 3600 cannot be used again. Moreover, the lockout 3690 can serve as a spent cartridge lockout.
  • a tool assembly 3700 comprises a staple cartridge 3720 and an anvil 3730.
  • the tool assembly 3700 further comprises a closure system configured to move the anvil 3730 toward the staple cartridge 3720 and, in addition, a firing system configured to eject, or fire, staples removably stored in the staple cartridge 3720.
  • the anvil 3730 comprises a longitudinal shaft portion 3736 and attachment arms 3738 extending from the shaft portion 3736 which are configured to resiliently grip a closure actuator, or trocar, 3734 of the closure system.
  • the closure actuator 3734 is retractable proximally by a closure drive to move the trocar 3734 between an open, unclamped position ( FIG. 59 ) and a closed, clamped position ( FIG. 60 ).
  • the closure system is in its open configuration, as illustrated in FIG. 59 , the staple firing system is disabled and cannot be actuated to fire the staples stored in the staple cartridge 3720, as described in greater detail below.
  • the staple firing system comprises a rotatable firing shaft 3750 comprising a threaded distal end and, in addition, a translatable firing nut 2550 comprising a threaded aperture configured to receive the threaded distal end of the firing shaft 3750.
  • a gap is present between the threaded distal end of the firing shaft 3750 and the threaded aperture defined in the firing nut 2550 when the anvil 3730 is in its open position.
  • the firing shaft 3750 cannot displace the firing nut 2550 distally until the firing shaft 3750 is threadably engaged with the firing nut 2550.
  • the attachment arms 3738 of the anvil 3730 are configured to engage the firing shaft 3750 and deflect the firing shaft 3750 outwardly when the anvil 3730 is moved into its closed position.
  • the attachment arms 3738 are configured to engage inwardly-extending projections 3758 defined on the firing shaft 3750 and push the projections 3758 and the perimeter of the firing shaft 3750 outwardly.
  • the threaded distal end of the firing shaft 3750 is pushed into operative engagement with the threaded aperture of the firing nut 2550 at a thread interface 3790 and, at such point, the firing shaft 3750 can displace the firing nut 2550 distally to eject the staples from the staple cartridge 3720 when the firing shaft 3750 is rotated by a firing drive.
  • the firing shaft 3750 will return to its original configuration and become operably disengaged from the firing nut 2550.
  • the tool assembly 3700 comprises a lockout which prevents the staples from being fired if the anvil 3730 is not attached to the closure system, if the anvil 3730 is improperly attached to the closure system, and/or if the anvil 3730 is not sufficiently closed.
  • a tool assembly 3800 comprises a replaceable staple cartridge including staples removably stored therein, an anvil configured to deform the staples, a closure drive system configured to move the anvil relative to the staple cartridge, and a firing system configured to eject the staples from the staple cartridge.
  • the tool assembly 3800 further comprises a lockout configured to prevent the firing system from being operated unless the staple cartridge is fully seated onto the tool assembly 3800.
  • the staple cartridge comprises a cartridge frame 3820 configured to engage a shaft frame 3810 of the tool assembly 3800.
  • the staple cartridge further comprises a drive shaft 3830 which is inserted into the shaft frame 3810 when the staple cartridge is assembled to the tool assembly 3800.
  • the drive shaft 3830 comprises a proximal end 3832 including an annular gear portion 3833 which is configured to engage and compress a transmission 3860 of the firing system when the staple cartridge is assembled to the tool assembly 3800.
  • the transmission 3860 comprises a first portion 3862, a second portion 3864, and a third portion 3868 which, when pushed into operative engagement with each other, are able to transmit a rotary input motion to the drive shaft 3830.
  • the annular gear portion 3833 of the drive shaft 3830 is configured to engage a corresponding gear portion 3863 defined on the distal side of the first transmission portion 3862 and, when the first transmission portion 3862 is pushed proximally by the drive shaft 3830, the first transmission portion 3862 can operably engage the second transmission portion 3864. More specifically, the first transmission portion 3862 comprises a proximal gear portion 3865 which engages a distal gear portion 3866 of the second transmission portion 3864 and, concurrently, pushes the second transmission portion 3864 proximally when the first transmission portion 3862 is pushed proximally by the drive shaft 3830.
  • the second transmission portion 3864 can operably engage the third transmission portion 3868. More specifically, the second transmission portion 3862 comprises a proximal gear portion 3867 which engages a distal gear portion 3869 of the third transmission portion 3864 when the first transmission portion 3862 and the second transmission portion 3864 are pushed proximally by the drive shaft 3830.
  • the third transmission portion 3868 is operably coupled to an input shaft and supported from being displaced proximally by the input shaft and/or the shaft housing 3810.
  • the transmission 3860 further comprises at least one spring member 3870 positioned intermediate the first transmission portion 3862 and the second transmission portion 3864.
  • the spring member 3870 can comprise one or more wave springs, for example.
  • the spring member 3870 is configured to bias the first transmission portion 3862 and the second transmission portion 3864 apart from one another.
  • the transmission 3860 further comprises at least one spring member 3870 positioned intermediate the second transmission portion 3864 and the third transmission portion 3868 which, similar to the above, is configured to bias the second transmission portion 3864 and the third transmission portion 3868 apart from one another.
  • each spring member 3870 comprises two disc springs 3872 which are configured to deflect when a compressive force is applied thereto; however, the springs members 3870 can comprise any suitable configuration.
  • the input shaft of the tool assembly 3800 can rotate the third transmission portion 3868; however, the rotation of the third transmission portion 3868 cannot be transmitted to the second transmission portion 3864 unless the spring member 3870 positioned intermediate the second transmission portion 3864 and the third transmission portion 3868 has been sufficiently compressed to connect the proximal gear portion 3867 of the second transmission portion 3864 with the distal gear portion 3869 of the third transmission portion 3868.
  • the second transmission portion 3864 cannot transmit rotary motion to the first transmission portion 3862 unless the spring member 3870 positioned intermediate the first transmission portion 3862 and the second transmission portion 3864 has been sufficiently compressed to connect the proximal gear portion 3865 of the first transmission portion 3862 and the distal gear portion 3866 of the second transmission portion 3864.
  • the drive shaft 3830 engages the first transmission portion 3862 with the second transmission portion 3864 and engages the second transmission portion 3864 with the third transmission portion 3868 when the staple cartridge is fully seated onto the shaft frame 3810, as illustrated in FIG. 62 . In such instances, the rotation of the input shaft can be transmitted to the drive shaft 3830.
  • the tool assembly 3800 assures that the staples stored within the staple cartridge cannot be ejected from the staple cartridge unless the staple cartridge is fully seated onto the shaft frame 3810.
  • a tool assembly 3900 comprises a shaft 3910 and a replaceable staple cartridge 3920.
  • the replaceable staple cartridge 3920 comprises a closure drive configured to move an anvil relative to the staple cartridge 3920 and, in addition, a firing drive comprising a rotatable firing shaft 3930 configured to eject staples removably stored in the staple cartridge 3920.
  • the tool assembly 3900 comprises a lockout configured to prevent the firing drive from ejecting the staples from the staple cartridge 3920 unless the staple cartridge 3920 is fully, or sufficiently, seated onto the shaft 3910.
  • the lockout prevents the firing shaft 3930 from rotating within the staple cartridge 3920 unless the staple cartridge 3920 is fully, or sufficiently, seated onto the shaft 3910.
  • the firing shaft 3930 comprises an annular array of lock apertures 3939 defined in the outer perimeter thereof and the staple cartridge 3920 comprises at least one lock 3929 configured to releasably engage a lock aperture 3939 defined in the shaft 3930.
  • the lock 3929 comprises a proximally-extending cantilever beam; however, any suitable configuration could be utilized.
  • the lock 3929 further comprises a locking projection that extends into the lock aperture 3939 and prevents the firing shaft 3930 from rotating, or at least substantially rotating, relative to the body of the staple cartridge 3920.
  • the lock 3929 is configured such that it is biased into engagement with a lock aperture 3939 defined in the firing shaft 3930 until the lock 3929 is lifted out of the lock aperture 3939 when the staple cartridge 3920 is fully, or sufficiently, assembled to the shaft 3910, as illustrated in FIG. 68 .
  • the outer housing of the shaft 3910 comprises a wedge 3919 configured to lift the lock 3929 away from the firing shaft 3930 and disengage the lock 3929 from the lock aperture 3939.
  • the wedge 3919 is configured such that it does not disengage the lock 3929 from the firing shaft 3930 unless the staple cartridge 3920 has been fully, or sufficiently, seated onto the shaft 3910, as illustrated in FIG. 68.
  • FIG. 67 illustrates a scenario where the staple cartridge 3920 has not been fully, or sufficiently, seated onto the shaft 3910.
  • a tool assembly 4000 comprises a shaft 4010 and a replaceable staple cartridge 4020.
  • the replaceable staple cartridge 4020 comprises a closure drive configured to move an anvil relative to the staple cartridge 4020 and, in addition, a firing drive comprising a rotatable firing shaft 3930 configured to eject staples removably stored in the staple cartridge 4020.
  • the staple cartridge 4020 comprises a lock 4029 configured to releasably connect the staple cartridge 4020 to the shaft 4010.
  • the lock 4029 comprises a proximally-extending cantilever and a lock shoulder 4028 extending therefrom.
  • the lock 4029 is configured to deflect inwardly within the shaft 4010 as the staple cartridge 4020 is assembled to the shaft 4010 and then resiliently return to, or at least toward, its undeflected state when the lock shoulder 4028 of the lock 4029 becomes aligned with a window 4019 defined in the outer housing of the shaft 4010. In such instances, the lock shoulder 4028 enters into the window 4019 when the staple cartridge 4020 has been fully, or sufficiently, seated on the shaft 4010, as illustrated in FIG. 70 .
  • a clinician can insert a tool or their finger, for example, into the window and depress the lock 4029 away from the window 4019. At such point, the staple cartridge 4020 can be removed from the shaft 4010 and, if the clinician so desires, and attach a new staple cartridge to the shaft 4010.
  • a surgical stapling system can comprise an electrical lockout configured to prevent the closure drive of the stapling system from clamping the anvil onto the tissue and/or prevent the firing drive from performing its firing stroke when a staple cartridge has not been fully, or sufficiently, seated onto the shaft of the stapling system.
  • the stapling system can comprise a sensor configured to detect whether a staple cartridge has been fully, or sufficiently, seated on the shaft and, in addition, an electrical motor configured to operate the firing drive. In the event that the sensor detects that a staple cartridge has not been fully, or sufficiently, attached to the shaft, the motor can be electrically de-activated.
  • the stapling system comprises a controller, such as a microprocessor, for example, which is in communication with the sensor and the electric motor.
  • the controller is configured to, one, permit the electric motor to be operated if the sensor detects a properly seated staple cartridge on the shaft and, two, prevent the electric motor from being operated if the sensor detects an improperly seated staple cartridge on the shaft.
  • a tool assembly kit 4100 comprises a shaft 4110 and a plurality of staple cartridges, such as 4120,4120', 4120", and 4120''', for example.
  • Each staple cartridge 4120, 4120', 4120", and 4120''' is configured to apply circular rows of staples having a different diameter.
  • the staple cartridge 4120''' is configured to apply staples in a pattern having a large diameter while the staple cartridge 4120 is configured to apply staples in a pattern having a small diameter.
  • different staple cartridges can deploy staples having different unformed heights.
  • staple cartridges that apply staples in larger patterns deploy staples having a larger undeformed height while staple cartridges that apply staples in smaller patterns deploy staples having a smaller undeformed height.
  • a staple cartridge can deploy staples having two or more unformed heights.
  • a staple cartridge selected from the plurality of staple cartridges can be assembled to the shaft 4110.
  • the tool assembly 4100 comprises a detection circuit 4190 configured to detect whether a staple cartridge is fully, or sufficiently, attached to the shaft 4110.
  • the detection circuit 4190 is not entirely contained within the shaft 4110; rather, a staple cartridge must be properly assembled to the shaft 4110 to complete the detection circuit 4190.
  • the detection circuit 4190 comprises conductors 4193 that extend through a passage 4192 defined in the frame of the shaft 4110 and/or along the outer housing of the shaft 4110. Referring primarily to FIG. 73 , each conductor 4193 is electrically coupled to an electrical contact 4194 defined in the distal end of the housing.
  • the staple cartridge 4120 for example, comprises corresponding electrical contacts 4195 which are positioned and arranged on the body 4122 of the staple cartridge 4120 such that the contacts 4195 engage the contacts 4194 on the shaft 4110.
  • the staple cartridge 4120 further comprises conductors 4196 extending through and/or along the cartridge body 4122. Each conductor 4196 is electrically coupled with a contact 4195. In certain instances, the conductors 4196 are directly coupled to one another and, in such instances, the detection circuit 4190 is closed once the staple cartridge 4120 is properly assembled to the shaft 4110.
  • the detection circuit 4190 of the tool assembly 4100 extends through a deck portion 4124 of the staple cartridge 4120.
  • the deck portion 4124 is movably attached to the cartridge body 4122.
  • spring members 4198 are positioned intermediate the cartridge body 4122 and the deck portion 4124 and are configured to permit the deck portion 4124 to move, or float, relative to the cartridge body 4122 when tissue is compressed against the deck portion 4124.
  • the spring members 4198 comprise one or more wave springs, for example.
  • the spring members 4198 also form an electrically conductive pathway between the cartridge body 4122 and the deck portion 4124.
  • the spring members 4198 are positioned intermediate electrical contacts 4197 and 4199 defined on the cartridge body 4122 and the deck portion 4124, respectively.
  • the conductors 4196 are electrically coupled to electrical contacts 4197 defined on the distal end of the cartridge body 4122 and the electrical contacts 4199 are electrically coupled to one another through a conductor in the deck portion 4125.
  • the detection circuit 4190 is closed once the staple cartridge 4120 is properly assembled to the shaft 4110.
  • a tool assembly 4200 comprises a lockout configured to prevent a replaceable circular staple cartridge from being fired more than once, as described in greater detail further below.
  • a replaceable circular staple cartridge 4220 is assembled to a shaft 4210 of the tool assembly 4200.
  • the tool assembly 4200 is then positioned in the surgical site and an anvil 2230 is assembled to the trocar 2450 of the closure drive.
  • the closure drive is then used to move the anvil 2230 toward the staple cartridge 4220 to clamp the patient's tissue against the staple cartridge 4220 until the anvil 2230 reaches a closed, or clamped, position. This position of the anvil 2230 is illustrated in FIG. 74 .
  • the firing drive can be operated to deploy the staples removably stored in the staple cartridge 4220.
  • the firing drive comprises, among other things, a rotatable drive shaft 4230 which is threadably engaged with a drive collar 4240 and, in addition, a staple firing driver 2560.
  • the drive collar 4240 and the firing driver 2560 comprise separate components; however, the drive collar 4240 and the firing driver 2560 could be integrally formed in alternative embodiments.
  • the firing drive is rotatable in a first direction during a firing stroke to push the drive collar 4240 and the staple firing driver 2560 distally between an unfired position ( FIG. 74 ) and a fired position ( FIG. 75 ) to eject the staples from the staple cartridge 4220.
  • the drive collar 4240 and the staple driver 2560 are prevented from rotating within the staple cartridge 4220 and, as a result, the drive shaft 4230 rotates relative to the drive collar 4240 and the staple driver 2560.
  • the drive collar 4240 comprises one or more lockouts 4290 extending proximally therefrom.
  • Each lockout 4290 comprises a lockout pin 4292 slidably positioned within a pin aperture 4293 defined in the drive collar 4240.
  • Each lockout 4290 further comprises a biasing member, such as a spring 4294, for example, configured to bias the pins 4292 proximally.
  • the lockout pins 4292 move away from the drive shaft 4230, as illustrated in FIG. 75 .
  • the drive shaft 4230 is rotated in an opposite direction to pull the drive collar 4240 and the staple driver 4260 proximally during a retraction stroke.
  • the lockouts 4290 are moved toward the drive shaft 4230.
  • the retraction stroke is longer than the firing stroke and, as a result, the drive collar 4240 is moved proximally with respect to its original unfired position into a retracted position, as illustrated in FIG. 76 .
  • each lockout 4290 has become engaged with the drive shaft 4230 and the frame 4222 ofthe staple cartridge 4220. More specifically, each lockout 4290 has entered into a lockout aperture defined between the drive shaft 4230 and the cartridge frame 4222. Referring now to FIG. 78 , each lockout aperture is defined by an aperture wall 4295 in the drive shaft 4230 and an aperture wall 4296 in the frame 4222. Once the lockout pins 4292 have entered the lockout apertures, the drive collar 4240 cannot be rotated by the drive shaft 4230 and the firing system of the staple cartridge 4220 has become locked out. As a result, that particular staple cartridge 4220 cannot be used again and must be replaced with a new staple cartridge in order for the tool assembly 4200 to be used again.
  • lockout pins 4292 may or may not be partially positioned in the lockout apertures when the firing drive is in its unfired configuration as illustrated in FIG. 74 . To the extent, however, that the lockout pins 4292 are partially positioned in the lockout apertures, in such instances, the pins 4292 can displace distally within the pin apertures 4293 defined in the drive collar 4240 when the firing drive shaft 4230 is rotated.
  • lockout pins 4292 are seated deeply enough into the lockout apertures defined in the drive shaft 4230 when the drive collar 4240 is moved into its retracted position so as to prevent the pins 4292 from being displaced distally out of the lockout apertures if the firing drive shaft 4230 is rotated in its first direction once again.
  • the sidewalls 4295 and 4296 of the lockout apertures are aligned with one another when the drive collar 4240 is in its retracted position.
  • the sidewalls 4295 defined in the drive shaft 4230 will rotate out of alignment with the sidewalls 4296 defined in the cartridge frame 4222.
  • the sidewalls 4295 may momentarily rotate into re-alignment with the sidewalls 4296 as the firing drive 4230 is rotated.
  • the sidewalls 4295 are not aligned with the sidewalls 4296 when the firing system is in its unfired configuration.
  • the lockout pins 4292 cannot enter into the lockout apertures when the firing system is in its unfired configuration and the staple cartridge 4220 cannot become unintentionally locked out.
  • one or more lockout apertures 4295" can be exclusively defined in a drive shaft 4230" of a tool assembly 4200".
  • the drive collar 4240 would not be able to rotate relative to the drive shaft 4230" once the lockout pins 4292 entered into the lockout apertures 4295".
  • the drive collar 4240 and the drive shaft 4230" would become synchronously locked together, but not necessarily locked to the frame of the tool assembly 4200", which would prevent the drive shaft 4230" from rotating relative to the drive collar 2440 and displacing the drive collar 2440 distally.
  • each of the firing drive lockouts has a different configuration such that each lockout pin is uniquely indexed with its corresponding lockout aperture.
  • the tool assembly 4200' comprises a first lockout pin configured to enter a first lockout aperture defined by sidewalls 4295 and 4296 and a second lockout pin configured to enter a second lockout aperture defined by sidewalls 4295' and 4296'.
  • the first lockout pin of the tool assembly 4200' is sized and configured such that it cannot enter into the second lockout aperture and, correspondingly, the second lockout pin is sized and configured such that it cannot enter into the first lockout aperture.
  • neither the first lockout pin nor the second lockout pin can enter an aperture formed by a combination of sidewalls 4295 and 4296' or an aperture formed by a combination of sidewalls 4295' and 4296.
  • a stapling instrument configured to deploy circular rows of staples can comprise an articulation joint.
  • the articulation joint is configured to permit an end effector of the stapling instrument to articulate relative to a shaft of the stapling instrument.
  • Such a stapling instrument can assist a surgeon in positioning the end effector within the rectum and/or colon of a patient.
  • a stapling instrument configured to deploy circular rows of staples such as stapling instrument 9000, for example, can be can comprise a contourable or adjustable frame 9010.
  • the frame 9010 can be configured to be permanently deformed during use.
  • the frame 9010 is comprised of a malleable metal, such as silver, platinum, palladium, nickel, gold, and/or copper, for example.
  • the frame 9010 is comprised of a malleable plastic, for example.
  • the frame is comprised of a polymer including metal ions bonded with the polymer chains, such as ionic polymer-metal composites (IPMCs), for example.
  • IPMCs ionic polymer-metal composites
  • a voltage potential, or potentials can be applied to the IPMC material in order to defect the shaft in a desired manner.
  • the shaft is contourable along one radius of curvature while, in other instances, the shaft is contourable along more than one radius of curvature.
  • the voltage potential, or potentials, can be modified to contour the shaft while the shaft is within the patient, for example.
  • the contourable portion of the frame comprises a plurality of pivotable links.
  • the contourable portion of the frame is comprised of a visco-elastic material.
  • the stapling instrument can further comprise a lock configured to releasably hold the contourable portion of the stapling instrument frame in its contoured configuration.
  • the stapling instrument frame comprises articulatable frame links and one or more longitudinal tension cables which can pull the frame links proximally and lock the frame links together.
  • each frame link can comprise a longitudinal aperture extending therethrough which is configured to receive a distally movable rod. The rod is sufficiently flexible to pass through the longitudinal apertures, which may not be completely aligned with one another when the contourable portion has been contoured, yet sufficiently rigid to hold the stapling instrument in its contoured configuration.
  • a surgical instrument can be comprised of a plurality of modules that are assembled to one another.
  • a surgical instrument comprises a first module including a handle and a second module including a shaft assembly.
  • the shaft assembly comprises an end effector configured to staple and/or incise the tissue of a patient; however, the shaft assembly can comprise any suitable end effector.
  • the end effector comprises a third module attachable to the shaft assembly.
  • a handle such as the handle 20, for example, comprises a controller and a display 10000 in communication with the controller.
  • the controller is configured to display data regarding the operation of the surgical instrument on the display 10000.
  • the data displayed on the display 10000 relates information to a surgeon regarding at least one operating parameter of the first module and/or at least one operating parameter of the second module.
  • the controller can display data on the display 10000 regarding the progress of the staple firing stroke.
  • the shaft assembly comprises a second display.
  • the shaft assembly 2000 comprises a display 10100; however, any of the shaft assemblies disclosed herein can comprise a display such as display 10100, for example.
  • the second module comprises its own controller configured to display data regarding the operation of the surgical instrument on the display 10100. Similar to the above, the data displayed on the display 10100 relates information regarding at least one operating parameter of the first module and/or at least one operating parameter of the second module.
  • the controller of the second module is in signal communication with the controller of the first module; however, in other embodiments, the second module controller can operate independently of the first module controller. In certain alternative embodiments, the second module does not comprise a controller. In such embodiments, the controller of the first module is in signal communication with the first display 10000 and the second display 10100 and controls the data displayed on the first display 10000 and the second display 10100.
  • the tool assembly 2000 comprises an anvil and a staple cartridge.
  • the handle 20 comprises an actuation system configured to move the anvil relative to the staple cartridge.
  • the anvil is positionable in a range of positions relative to the staple cartridge to control the distance, or gap, between the anvil and the staple cartridge and, as a result, control the forming height of the staples when the staples are ejected from the staple cartridge. For instance, the anvil is positioned closer to the staple cartridge to deform the staples to a shorter formed height and positioned further away from the staple cartridge to deform the staples to a taller formed height.
  • the second display 10100 of the tool assembly 2000 is configured to display the position of the anvil relative to the staple cartridge and/or display the height in which the staples will be or have been formed.
  • a shaft assembly can comprise an actuator configured to control a function of the end effector and a display which displays data regarding the end effector function which is adjacent to the actuator.
  • a tool assembly 1500 comprises a shaft and an end effector extending from the shaft.
  • the shaft comprises a shaft frame a longitudinal shaft axis.
  • the end effector comprises an end effector frame and a longitudinal end effector axis.
  • the end effector further comprises a distal head and a rotation joint which permits the distal head to rotate relative to the end effector frame about the longitudinal end effector axis.
  • the distal head comprises a first jaw and a second jaw.
  • the first jaw comprises a staple cartridge including staples removably stored therein, or a channel configured to receive such a staple cartridge, and the second jaw comprises an anvil configured to deform the staples.
  • the second jaw is movable relative to the first jaw between an open position and a closed position; however, other embodiments are envisioned in which the first jaw is movable relative to the second jaw and/or both the first jaw and the second jaw are movable relative to each other.
  • a tool assembly can comprise an articulation joint in addition to the rotation joint.
  • the rotation joint is distal with respect to the articulation joint.
  • the rotation of the distal head does not affect the angle in which the end effector has been articulated. That said, other embodiments are envisioned in which the articulation joint is distal with respect to the rotation joint. Such embodiments can provide a wide sweep of the distal head.
  • the longitudinal end effector axis is movable relative to the longitudinal shaft axis. In at least one instance, the longitudinal end effector axis is movable between a position in which it is collinear with the longitudinal shaft axis to a position in which it is transverse to the longitudinal shaft axis.
  • the distal head of the tool assembly 1500 is rotatable between an initial position and a rotated position. In at least one instance, the distal head is rotatable between a zero, or top-dead-center, position and a second position. In certain instances, the distal head is rotatable through an at least 360 degree range of motion. In other instances, the distal head is rotatable through a less than 360 degree range of rotation. In either event, the tool assembly 1500 and/or the handle 20 is configured to track the rotational position of the distal head.
  • the tool assembly 1500 and/or the handle 20 comprises an electric motor operably coupled with the distal head of the end effector and, in addition, an encoder configured to directly track the rotation of the distal head and/or indirectly track the rotation of the distal head by evaluating the rotational position of the shaft of the electric motor, for example.
  • the controller of the handle 20 is in signal communication with the encoder and is configured to display the rotational position of the distal head on the display 10000, for example.
  • the orientation and the arrangement of the data displayed on the display 10000 is static while the distal head of the end effector rotates.
  • the data displayed on the display 10000 in such an embodiment would be updated by the surgical instrument controller; however, the data display is not re-oriented and/or re-arranged as the distal head rotates.
  • the data field on the display 10000 is dynamic.
  • dynamic means more than the data being updated on the display 10000; rather, the term dynamic means that the data is re-oriented and/or re-arranged on the display 10000 as the distal head is rotated.
  • the orientation of the data tracks the orientation of the distal head. For example, if the distal head is rotated 30 degrees, the data field on the display 10000 is rotated 30 degrees. In various instances, the distal head is rotatable 360 degrees and the data field is rotatable 360 degrees.
  • the data field can be oriented in any orientation that matches the orientation of the distal head.
  • the controller orients the data field in an orientation selected from an array of discrete positions that most closely matches the orientation of the distal head. For instance, if the distal head has been rotated 27 degrees and the selectable discrete data field positions are 15 degrees apart, the controller can re-orient the data field 30 degrees from a datum orientation. Similarly, for example, if the distal head has been rotated 17 degrees and the selectable discrete data field positions are 5 degrees apart, the controller can re-orient the data field 15 degrees from the datum orientation.
  • the datum orientation is aligned with a feature of the surgical instrument itself.
  • the datum orientation of the handle 20 is aligned with an axis extending through a grip of the handle 20.
  • the controller can disregard the orientation of the handle 20 with respect to its environment.
  • the datum orientation is aligned with respect to the gravitational axis, for example.
  • the controller is configured to re-orient the entire data field displayed on the display 10000 with respect to the orientation of the distal head. In other embodiments, the controller is configured to re-orient only a portion of the data field displaced on the display 10000 with respect to the orientation of the distal head. In such an embodiment, a portion of the data field is held static with respect to the datum orientation while another portion of the data field is rotated with respect to the datum orientation. In certain embodiments, a first portion of the data field is rotated a first angle of rotation and a second portion of the data field is rotated a second angle of rotation in the same direction. For instance, the second portion can be rotated less than the first portion. In various embodiments, a first portion of the data field is rotated in a first direction and a second portion of the data field is rotated in a second, or opposite, direction.
  • the data field is re-oriented and/or re-arranged in real time, or at least substantially in real time, with the rotation of the distal head.
  • Such an embodiment provides a very responsive data display.
  • the re-orientation and/or re-arrangement of the data field can lag the rotation of the distal head.
  • Such embodiments can provide a data display with less jitter.
  • a first portion of the data field is re-oriented and/or re-arranged at a first speed and a second portion of the data field is re-oriented and/or re-arranged at a second, or different, speed. For instance, the second potion can be rotated at a slower speed.
  • the data field on the display 10000 is rotated as the distal head of the end effector is rotated.
  • the data field, or a portion of the data field is translated as the distal head is rotated.
  • the controller of the surgical instrument is configured to re-orient and/or re-arrange the data field on the handle display 10000.
  • the controller of the surgical instrument can re-orient and/or re-arrange the data field on a second display, such as a shaft display, for example.
  • the tool assembly 2000 comprises an actuator 10200 configured to actuate the articulation drive system of the tool assembly 2000.
  • the actuator 10200 is rotatable about a longitudinal axis which is parallel to, or at least substantially parallel to, a longitudinal axis of the shaft 2100, for example.
  • the actuator 10200 is operably coupled to a rheostat, for example, which is in signal communication with a controller of the handle 20.
  • the rheostat detects the rotation of the actuator 10200 and the controller operates the electric motor to articulate the end effector 2200 in a first direction.
  • the rheostat detects the rotation of the actuator 10200 and the controller operates the electric motor to articulate the end effector 2200 in a second, or opposite, direction.
  • the end effector 2200 can be articulated approximately 30 degrees from a longitudinal axis in a first direction and/or articulated approximately 30 degrees from the longitudinal axis in a second, or opposite, direction, for example.
  • the tool assembly 2000 does not have an on-board electric motor configured to operate the articulation drive system; rather, the electric motor of the articulation drive system is in the handle, such as handle 20, for example, to which the tool assembly 2000 is attached.
  • an actuator on the detachable shaft assembly controls the operation of the handle.
  • the electric motor of the articulation driver system can be in the tool assembly 2000.
  • the display 10100 is configured to display, in at least some manner, the articulation of the end effector 2200. As the reader should appreciate, the display 10100 is adjacent the actuator 10200 and, as a result, the surgeon is able to easily view the input and the output of the articulation drive system at the same time.
  • a surgical tool assembly comprising a contourable shaft, further to the above, can be advantageously shaped to fit within the rectum or colon of a patient, for example.
  • a contourable shaft cannot bear a significant amount of tensile and/or compressive loads.
  • only rotatable drive systems may extend through the contourable portion of the shaft.
  • the shaft need only resist the rotational reaction forces generated by the rotatable drive systems.
  • the rotational motion of the drive systems can be converted to linear motion, if necessary, distally with respect to the contourable shaft portion.
  • Such longitudinal motions can generate tensile and/or compressive forces; however, such forces can be resolved, or balanced out, within the end effector, i.e., distally with respect to the contourable shaft portion.
  • Such embodiments can also utilize an articulation joint positioned distally with respect to the contourable shaft portion.
  • the tool assembly may not utilize push-pull drive systems which traverse the contourable shaft portion.
  • FIGS. 84 and 85 An anvil 6020 of a circular stapling instrument is illustrated in FIGS. 84 and 85 .
  • the anvil 6020 comprises a tissue compression surface 6022 and an annular array of staple forming pockets 6024 defined in the tissue compression surface 6022.
  • the anvil 6020 further comprises a frame 6028, an attachment mount 6026, and a stem extending from the attachment mount 6026.
  • the stem is configured to be releasably attached to a closure drive of the circular stapling instrument so that the anvil 6020 can be moved toward and away from a staple cartridge of the circular stapling instrument.
  • the compression surface 6022, the attachment mount 6026, and the frame 6028 are comprised of stainless steel, for example; however, any suitable material, or materials, could be used.
  • the anvil 6020 comprises a tissue support 6030.
  • the tissue support 6030 is positioned within an annular aperture defined within the tissue support surface 6022.
  • the tissue support 6030 is snugly secured within the anvil 6020 such that there is little, if any, relative movement therebetween.
  • the tissue support 6030 comprises an annular tissue support surface 6032 which is adjacent to the annular tissue compression surface 6022 of the anvil 6020.
  • the tissue support 6030 further comprises an inner annular wall 6036 defined therein and, in addition, a bottom wall 6038 positioned adjacent the anvil frame 6028 of the anvil 6020.
  • the circular stapling instrument comprises a staple cartridge 6040 including a first annular row of staples 6070, a second annular row of staples 6080, and a firing drive configured to eject the staples 6070 and 6080 from the staple cartridge 6040 during a firing stroke of the firing drive.
  • the staples 6070 and 6080 are deformed by the forming pockets 6024 as they are ejected from the staple cartridge 6040.
  • the staples 6070 and the staples 6080 are deformed to the same height while, in other instances, the staples 6070 and the staples 6080 are deformed to different heights.
  • the staples 6070 can be deformed to a shorter deformed height than the staples 6080.
  • the staples 6080 are deformed to a shorter height than the staples 6070.
  • the staples 6070 and the staples 6080 can have different unformed heights.
  • the staples 6070 can have a shorter unformed height than the staples 6080.
  • the staples 6080 have a shorter unformed height than the staples 6070.
  • the staples 6070 and the staples 6080 have the same unformed height.
  • the stapling instrument can incise the tissue T.
  • the firing drive which ejects the staples from their staple cavities, drives a cutting member 6050 toward the tissue T and the anvil 6020.
  • the distal edge of the cutting member 6050 transects the tissue T and then slides along the inner sidewall 6036 of the tissue support 6030 without transecting the inner sidewall 6036.
  • the cutting edge of the cutting member 6050 is annular and it is aligned with the annular inner wall 6036 of the tissue support 6030.
  • the cutting member 6050 is advanced into the anvil 6020 until the cutting member 6050 transects the bottom wall 6038, as illustrated in FIG. 86 .
  • the firing drive experiences various loads when driving the staples 6070 and 6080 against the anvil 6020 and/or cutting the tissue.
  • the firing drive may experience an increased load when transecting tissue that has been previously stapled, such as with staples 6090 ( FIG. 86 ), for example.
  • the transection of the bottom wall 6038 by the cutting member 6050 creates a sudden change or impulse in the force transmitted through the firing drive. This sudden change by the force can be sensed by the clinician using the surgical stapler and/or an electronic sensor system configured to detect load changes in the firing drive.
  • the tissue support 6030 can be comprised of a material that can snap when the cutting member 6050 applies a load to the bottom wall 6038. In at least one instance, the tissue support 6030 is comprised of plastic, for example. In any event, the transection of the bottom wall 6038 can be detected and, once detected, the clinician and/or the electronic sensor system can determine that the cutting process has been completed.
  • the firing drive deforms the staples 6070, 6080 and incises the tissue with the cutting member 6050 at the same time; however, it is contemplated that the staple forming and tissue cutting steps could be staggered. In at least one instance, the tissue cutting step does not begin until the staple forming step has been completed.
  • the cutting member 6050 can push the tissue T into the cavity defined between the inner wall 6036 of the tissue support 6030 and the attachment mount 6026 when the cutting member 6050 is moved toward the bottom wall 6038. Stated another way, the cutting member 6050 can drag the tissue T along the wall 6036 before finally cutting it. In such instances, the incision made by the cutting member 6050 may not be precise. Discussed below are improvements to the embodiment disclosed in FIG. 86 .
  • the tissue support 6130 comprises a first, or outer, annular wall 6131and a second, or inner, annular wall 6133.
  • the inner wall 6133 defines an aperture 6136 configured to closely receive the attachment mount 6026.
  • the outer wall 6131 and the inner wall 6133 are connected by lateral walls 6132.
  • the lateral walls 6132 extend radially around a center of the tissue support 6130 between the inner wall 6133 and the outer wall 6131.
  • the lateral walls 6132 are evenly spaced apart from one another; however, alternative embodiments are contemplated in which the lateral walls 6132 are not evenly spaced apart from one another.
  • each cavity 6134 can be enclosed on every side but the side facing the tissue, for example. In other instances, the side of the cavity facing the tissue can be enclosed.
  • the outer wall 6131 and the inner wall 6133 of the tissue support 6130 are configured to support the tissue as the tissue is being transected by the cutting member 6050.
  • the lateral walls 6132 also support the tissue and, in addition, block or resist the tissue from sliding relative to the outer wall 6131 and the inner wall 6133 as the tissue is being transected. It should be understood that the tissue can enter the cavities 6134 when the tissue is being transected; however, the relative movement between the tissue and the sidewalls can be greatly reduced.
  • the composition and arrangement of the lateral walls 6132 can be selected to provide more support to the tissue or less support to the tissue depending on the amount of support that is desired. For instance, thicker lateral walls 6132 can provide more tissue support than thinner lateral walls 6132. Similarly, more lateral walls 6132 can provide more tissue support than thinner lateral walls 6132.
  • the cutting member 6050 cuts the tissue and transects the lateral walls 6132.
  • the cutting member 6050 is annular and transects the lateral walls 6132 adjacent the outer wall 6131; however, a cutting member could transect the walls 6132 at any suitable location.
  • the lateral walls 6132 support the tissue before, during, and after the tissue is cut and prevent, or at least reduce the possibility of, the tissue being dragged along the outer wall 6131 and/or the inner wall 6133.
  • the tissue support 6130 comprises a bottom wall 6138 that is transected at the end of the cutting stroke.
  • a surgical stapler comprising a staple cartridge 6240 and an anvil 6220 is disclosed in FIGS. 89 and 90 .
  • the staple cartridge 6240 is similar to the staple cartridge 6040 in many respects.
  • the anvil 6220 is similar to the anvil 6020 and the anvil 6120 in many respects.
  • the anvil 6220 comprises an attachment stem 6226 and an annular tissue support 6230 positioned around the attachment stem 6226.
  • the tissue support 6230 comprises a central aperture configured to closely receive the stem 6226.
  • the tissue support 6230 further comprises an annular outer wall 6231 positioned adjacent the tissue compression surface of the anvil 6220 and, in addition, lateral walls 6232 extending radially from the outer wall 6231.
  • the tissue support 6230 does not comprise an inner annual wall and the inner ends of the lateral walls 6232 are free to deflect.
  • the tissue support 6230 further comprises a bottom wall 6238 which is incised by the cutting member 6050, similar to the above.
  • FIGS. 91 and 92 A surgical stapler comprising the staple cartridge 6240 and the anvil 6220 is illustrated in FIGS. 91 and 92 .
  • the tissue support 6230 of the anvil 6220 has been replaced with a tissue support 6330.
  • the tissue support 6330 comprises an annular central aperture configured to closely receive the stem 6226.
  • the tissue support 6330 further comprises a top wall 6332, a bottom wall 6338, and sidewalls 6336 extending between the top wall 6332 and the bottom wall 6338.
  • the top wall 6332 and the bottom wall 6338 are parallel, or at least substantial parallel; however, embodiments are envisioned in which the walls 6332 and 6338 are not parallel.
  • the sidewalls 6336 are parallel, or at least substantial parallel; however, embodiments are envisioned in which the sidewalls 6336 are not parallel.
  • the walls 6332, 6336, and 6338 define an annular cavity 6334 therebetween.
  • the cavity 6334 is enclosed, or at least substantially enclosed, on all sides.
  • the cavity 6334 extends uninterrupted around the stem 6226; however, other embodiments are envisioned in which the cavity 6334 is interrupted by sidewalls and/or changes in geometry, for example.
  • the tissue support 6330 is configured to support the tissue as the tissue is being transected by the cutting member 6050.
  • the tissue support 6330 is closely received within the anvil 6220 such that the tissue support 6330 does not move, or at least substantially move, relative to the anvil 6220.
  • the tissue support 6330 comprises a rigid box-shaped cross-section such that the deflection of the tissue support 6330 is minimized or insubstantial while the cutting member 6050 is transecting the tissue.
  • a gap is present between the bottom wall 6338 and the inner side wall 6336. Such a gap can provide some flexibility in the tissue support 6330; however, other embodiments are envisioned in which no such gaps are present.
  • the tissue support 6330 is comprised of plastic, for example; however, in various embodiments, the tissue support 6330 can be comprised of a flexible and/or elastomeric material, for example.
  • the cutting member 6050 transects the tissue support 6330 during its cutting stroke. As illustrated in FIG. 92 , the cutting member 6050 transects the top wall 6332 after transecting the tissue and then enters into the cavity 6334.
  • the top wall 6332 comprises an annular notch 6333 defined therein which is aligned with the annular cutting edge of the cutting member 6050.
  • the notch 6333 reduces the cross-section of the top wall 6332 and facilitates the incision of the top wall 6332.
  • the cutting member 6050 can also transect the bottom wall 6338 during its cutting stroke.
  • the transection of the top wall 6332 and the bottom wall 6338 of the tissue support 6330 can create force pulses in the firing drive of the stapling instrument.
  • the top wall 6332 and the bottom wall 6338 can be structurally configured to provide different pulses so that the clinician and/or electronic sensor system of the surgical instrument can discern the difference between the pulses and not incorrectly interpret the incision of the top wall 6332 as the end of the firing/cutting stroke.
  • the top wall 6332 of the tissue support 6330 is aligned, or at least substantially aligned, with the tissue compression surface 6022 of the anvil 6220.
  • the top wall 6332 can be recessed with respect to the tissue compression surface 6022 and/or extend above the tissue compression surface 6022.
  • the top wall 6332 of the tissue support extends above the forming surfaces 6024 of the anvil 6220.
  • the top wall 6332 can be recessed with respect to the forming surfaces 6024 and/or aligned with the forming surfaces 6024.
  • FIGS. 93 and 94 A surgical stapler comprising the staple cartridge 6240 and the anvil 6220 is illustrated in FIGS. 93 and 94 .
  • the tissue support 6430 comprises an annular central aperture configured to closely receive the stem 6226.
  • the tissue support 6430 further comprises a top wall 6432, a bottom wall 6438, and sidewalls 6436 extending between the top wall 6432 and the bottom wall 6438.
  • the walls 6432, 6436, and 6438 define an annular cavity 6434 therebetween.
  • the cavity 6434 is enclosed, or at least substantially enclosed, on all sides.
  • the cavity 6434 extends uninterrupted around the stem 6226; however, other embodiments are envisioned in which the cavity 6434 is interrupted by sidewalls and/or changes in geometry, for example.
  • the tissue support 6430 is configured to support the tissue as the tissue is being transected by the cutting member 6050.
  • the tissue support 6430 is closely received within the anvil 6220 such that the tissue support 6430 does not move, or at least substantially move, relative to the anvil 6220.
  • the tissue support 6430 comprises a rigid polygonal cross-section such that the deflection of the tissue support 6430 is minimized or insubstantial while the cutting member 6050 is transecting the tissue.
  • a gap is present between the bottom wall 6438 and the inner side wall 6436. Such a gap can provide some flexibility in the tissue support 6430; however, other embodiments are envisioned in which no such gaps are present.
  • the tissue support 6430 is comprised of plastic, for example; however, in various embodiments, the tissue support 6430 can be comprised of a flexible and/or elastomeric material, for example.
  • the inner sidewall 6436 is shorter than the outer sidewall 3436; however, other embodiments are envisioned in which the outer sidewall 6436 is shorter than the inner sidewall 6436.
  • the top wall 6432 is not parallel to the bottom wall 6438. More specifically, the top wall 6432 comprises an inclined portion which extends transversely to the bottom wall 6438 and/or other portions of the top wall 6432.
  • the cutting member 6050 transects the tissue support 6430 during its cutting stroke. As illustrated in FIG. 94 , the cutting member 6050 transects the top wall 6432 after transecting the tissue and then enters into the cavity 6434. The cutting member 6050 can also transect the bottom wall 6438 during its cutting stroke.
  • the tissue supports disclosed herein are configured to support tissue as the tissue is being incised by a cutting member.
  • the tissue being incised by the cutting member has been previously stapled, i.e., stapled during an earlier step in the surgical procedure, for example.
  • staples may also be incised by the cutting member even though they are comprised of metal, such as titanium and/or stainless steel, for example.
  • such staples may not be incised by the cutting member; rather, they may be pushed into the material comprising the tissue support.
  • the tissue supports disclosed herein comprise a sufficient strength and/or stiffness that prevents a staple trapped against the tissue support by the cutting member from creating more than localized plastic deformation in the tissue support.
  • the localized plastic deformation is limited to less than one characteristic length (CL) of the staple in any direction with respect to the staple.
  • the material of the tissue support can be selected such that the staple trapped against the tissue support may only create a zone of plastic deformation in the tissue support that has a diameter of less than 2*CL, for example.
  • the material of the tissue support can be selected such that the staple trapped against the tissue support may only create a zone of plastic deformation in the tissue support that has a diameter of less than 1.5*CL, for example.
  • a characteristic length of a staple can be the width of the staple crown, or backspan, and/or the formed height of the staple legs in their deformed configuration, for example.
  • the tissue supports disclosed herein can be comprised of a material which is sufficiently hard enough to support the staples as they are being incised by the cutting member. In at least one instance, the hardness of the material comprising the tissue support is equal to or greater than the hardness of the material comprising the staples being incised against the tissue support.
  • the hardness of the material comprising the tissue support is less than the hardness of the material comprising the staples being incised; however, the structural design of the tissue support is sufficient to prevent the tissue support from plastically stretching beyond an acceptable zone of plastic deformation.
  • the energy needed to incise the tissue and the formed staples in the tissue is less than the energy needed to incise the tissue support.
  • the material comprising the tissue support may be resistant to being gouged by the staples.
  • a biocompatible lubricant may be placed on and/or impregnated within the tissue support to prevent the staples from catching on the tissue support.
  • the tissue compression surface of an anvil and the tissue contacting surface of a tissue support are flat, or at least substantially flat. Such an arrangement can distribute the force applied by the anvil onto the tissue over a large area. Other embodiments are envisioned in which the tissue compression surface of the anvil and/or the tissue contacting surface of the tissue support are not flat.
  • the tissue compression surface of an anvil and/or the tissue contacting surface of a tissue support comprise tissue gripping members, or spikes, extending therefrom which are configured to engage and grip tissue. Such tissue gripping members can reduce relative movement, or slipping, between the tissue and the anvil, for example.
  • the density of the tissue gripping members on the tissue compression surface of the anvil and the tissue contacting surface of the tissue support is the same. In other instances, the density of the tissue gripping members on the tissue contacting surface of the tissue support is higher than the density of the tissue gripping members on the compression surface of the anvil. As the tissue support is positioned radially inwardly with respect to the compression surface of the anvil, the tissue gripping members can prevent the tissue from flowing or sliding radially inwardly in such an instance.
  • the anvil 6520 comprises a tissue compression surface 6522 and, in addition, forming pockets defined in the tissue compression surface 6522 which are configured to deform staples into a desired configuration when the staples are ejected from their staple cartridge.
  • Each forming pocket comprises a pair of cups, wherein each pair of cups is configured to deform the legs of a staple.
  • a pair of forming cups can include a first forming cup 6530a configured to deform the first leg of a staple and a second forming cup 6530b configured to deform the second leg of the staple.
  • the first forming cup 6530a and the second forming cup 6530b are mirror images of one another with respect an axis 6531 extending between the first forming cup 6530a and the second forming cup 6530b; however, other arrangements can be utilized.
  • the first forming cup 6530a comprises a first, or outer, end 6532 and a second, or inner, end 6534.
  • the first forming cup 6530a further comprises a bottom, or bathtub, surface 6536 extending between the outer end 6532 and the inner end 6534.
  • the first end 6532 is configured to receive the leg of a staple and begin the forming process of the leg.
  • the first end 6532 comprises a curved surface configured to deflect the staple leg toward the second end 6534.
  • the bottom surface 6536 comprises a curved, or concave, surface configured to at least partially turn the staple leg back toward the staple cartridge.
  • the second end 6534 comprises a curved surface which is configured to guide the staple leg out of the forming cup 6530a.
  • the second forming cup 6530b comprises a similar construction to that of the first forming cup 6530a and is configured to deform a second leg of the staple.
  • the first forming cup 6530a guides the first leg of the staple toward the second leg and the second forming cup 6530b guides the second leg of the staple toward the first leg.
  • the first forming cup 6530a and the second forming cup 6530b co-operate to deform the staple into a B-shaped configuration, for example; however, the forming cups can be configured to deform a staple into any suitable configuration.
  • each forming cup 6530 (6530a and 6530b) comprises a first lateral sidewall 6537 and a second lateral sidewall 6539 extending between the first end 6532 and the second end 6534.
  • the first lateral sidewall 6537 and the second lateral sidewall 6539 are mirror images of one another with respect to a longitudinal axis 6533 extending through the center of the forming cup 6530.
  • the first lateral sidewall 6537 and the second lateral sidewall 6539 are not mirror images of each other.
  • the sidewalls 6537, 6539 are sloped or inclined so as to guide the staple leg toward the center of the forming cup, i.e., toward the axis 6533, for example.
  • Each forming cup 6530 comprises a groove or channel 6538 defined in the bottom surface 6536 thereof.
  • the groove 6538 extends longitudinally between the first end 6532 and the second end 6534 of the forming cup 6530.
  • the groove 6538 extends parallel to, and laterally offset with respect to, a central longitudinal axis 6535 of the forming cup 6530.
  • the groove 6538 is wider than the leg of the staple that is deformed by the forming cup 6530; however, other embodiments are envisioned in which the groove 6538 is narrower than the leg of the staple. In either event, the groove 6538 is configured to guide the staple leg along a predetermined path within the forming cup 6530.
  • the grooves of the forming cups 6530 are configured to twist the legs of the staple while the legs are being deformed.
  • a staple is planar, or at least substantially planar, before it is deformed.
  • the legs and the base of the staple lie in the same plane which is aligned with the longitudinal axis 6535 when the staple is ejected from the staple cartridge.
  • the first ends 6532 and the bottom surfaces 6536 are sloped and/or otherwise configured to guide the legs toward the grooves 6538 when the staple legs enter into the forming cups 6530. Once the staple legs enter into the grooves 6538, the grooves 6538 will twist the staple legs out of plane with the base of the staple.
  • the unformed staple configuration is planar but the formed staple configuration is non-planar.
  • Other embodiments are envisioned, however, in which a staple has a non-planar configuration before and after it has been deformed.
  • the grooves 6538 of the forming cups 6530 are positioned on the same side of the longitudinal axis 6535 and are configured to twist both of the staple legs to the same side of the staple base.
  • Other embodiments, however, are envisioned in which a first staple leg is twisted to one side of the staple base and a second staple leg is twisted to another side of the staple base.
  • a first groove 6538 is positioned on a first side of the longitudinal axis 6535 that is configured to twist a first staple leg to a first side of the staple base while a second groove 6538 is positioned on a second side of the longitudinal axis 6535 that is configured to twist a second staple leg to a second side of the staple base.
  • the grooves 6538 of the forming cups 6530 are collinear, or at least substantially collinear. Other embodiments, however, are envisioned in which the grooves 6538 are positioned on the same side of the longitudinal axis 6535 but are not collinear with each other. In at least one such instance, the grooves 6538 are parallel to each other while, in other such instances, the grooves 6538 are not parallel to each other.
  • the groove 6538 is deeper than the bottom surface 6536 of the forming cup 6530.
  • Other embodiments, however, are envisioned in which the groove and the bottom surface of a forming cup have the same depth.
  • the forming cups 6530 are arranged in longitudinal rows when the anvil 6520 is part of a longitudinal end effector configured to apply longitudinal rows of staples.
  • the grooves 6538 of the forming cups are arranged such all of the staples deployed by the end effector are bent out of plane in the same direction.
  • the grooves 6538 are arranged in a first longitudinal row of forming cups 6530 to bend the staple legs in a first direction and a second longitudinal row of forming cups 6530 to bend the staple legs in a second, or different, direction.
  • the grooves 6538 are arranged to bend the legs of a first staple in a staple row in a first direction and a second staple in the staple row in a second, or opposite, direction.
  • the forming cups 6530 are arranged in annular rows when the anvil 6520 is part of an annular end effector configured to apply annular rows of staples.
  • the grooves 6538 are positioned radially outwardly with respect to the center longitudinal axes 6535 of the forming cups 6530.
  • the grooves 6538 are positioned radially inwardly with respect to the center longitudinal axes 6535 of the forming cups 6530.
  • the grooves 6538 are positioned radially outwardly in a first annular row of forming cups 6530 and radially inwardly in a second annular row of forming cups 6530.
  • a forming pocket of an anvil can comprise any suitable configuration.
  • a forming pocket can comprise two forming cups which are mirror images of each other with respect to a central axis.
  • Each forming cup comprises a triangular configuration having an outer end and an inner end. The inner ends of a pair of forming cups are adjacent to each other. The outer ends of the forming cups are wider than the inner ends and are configured to receive the legs of a staple.
  • Each forming cup further comprises a bottom, or bathtub, surface extending between the outer end and the inner end and, in addition, a longitudinal groove defined in the bottom surface configured to guide the staple leg within the forming cup. In at least one instance, the longitudinal groove is centered in the bottom surface of the forming cup.
  • FIGS. 97-99 An end effector 7000 of a circular stapling assembly is disclosed in FIGS. 97-99 .
  • the end effector 7000 comprises a staple cartridge including a deck 7030 and a cartridge body 7040.
  • the deck 7030 comprises a tissue compression surface 7031 and staple cavities 7032 defined in the compression surface 7031.
  • the staple cavities 7032 are arranged in a first, or inner, annular row and a second, or outer, annular row.
  • Each staple cavity 7032 in the inner row comprises a first staple 7070a removably stored therein and each staple cavity 7032 in the outer row comprises a second staple 7070b removably stored therein.
  • the end effector 7000 further comprises staple drivers which are configured to push the staples out of the staple cartridge.
  • the staple cartridge comprises a first annular row of staple drivers 7060a configured to eject the first row of staples 7070a and a second annular row of staple drivers 7060b configured to eject the second row of staples 7070b cartridge body 7040.
  • the staple drivers 7060a and 7060b are positioned within and/or aligned with the staple cavities 7032 defined in the deck 7030.
  • the staple drivers 7060a and 7060b are slidable within the staple cavities 7032 to eject the staples 7070a and 7070b, respectively, from the staple cavities 7032.
  • the end effector 7000 further comprises an anvil 7020.
  • the anvil 7020 comprises a tissue compression surface 7021 and staple forming pockets 7022 defined in the compression surface 7021.
  • the staple forming pockets 7022 are arranged in a first, or inner, annular row and a second, or outer, annular row.
  • the staple forming pockets 7022 are aligned with the staple cavities 7032 such that the staples 7070a, 7070b contact the staple forming pockets 7022 when the staples 7070a, 7070b are ejected from the staple cavities 7032.
  • the end effector 7000 further comprises a firing member 7056 configured to lift the staple drivers 7060a and 7060b within the staple cavities 7032 to eject the staples 7070a and 7070b, respectively, from the staple cavities 7032.
  • the firing member 7056 comprises a base 7054 and a ramp 7055.
  • the base 7054 is slidably positioned within a recess 7052 defined in a firing drive 7050.
  • the ramp 7055 is slidably positioned within a slot 7041 defined in the cartridge body 7040. As described in greater detail below, the ramp 7055 is configured to slide within the slot 7041 and progressively contact the staple drivers 7060a, 7060b to eject the staples 7070a, 7070b from the staple cavities 7032.
  • the firing member 7056 is movable through a firing stroke to eject the staples 7070a, 7070b from the staple cavities 7032. During the firing stroke, the firing member 7056 is moved along a curved, or arcuate, path which is defined by the slot 7041. Referring primarily to FIG. 97 , the slot 7041 comprises a first end 7042 and a second end 7049 and a continuous path therebetween. The ramp 7055 of the firing member 7056 is positioned in the first end 7042 at the beginning of the firing stroke and the second end 7049 at the end of the firing stroke.
  • the first end 7042 of the slot 7041 is aligned with the inner row of staple cavities 7032 and the second end 7049 of the slot 7041 is aligned with the outer row of staple cavities 7032.
  • the slot 7041 further comprises a first circumferential portion 7043 that extends around a central longitudinal axis 7090 extending through the end effector 7000.
  • the first circumferential portion 7043 of the slot 7041 is aligned with and extends under the staple drivers 7060a in the inner row of staple cavities 7032.
  • the ramp 7055 of the firing member sequentially engages the staple drivers 7060a to sequentially fire the staples 7070a as the firing member 7056 moves through the first circumferential portion 7043 of the slot 7041.
  • the first circumferential portion 7043 is defined by a constant, or at least substantially constant, radius of curvature about the longitudinal axis 7090; however, other embodiments are envisioned in which the radius of curvature of the first circumferential portion 7043 is not constant. In at least one such instance, the first circumferential portion 7043 comprises a spiral. Stated another way, in such an instance, the first circumferential portion 7043 recedes away from the longitudinal axis 7090 as it extends around the longitudinal axis 7090.
  • the second circumferential portion 7045 of the slot 7041 is aligned with and extends under the staple drivers 7060b in the outer row of staple cavities 7032.
  • the ramp 7055 ofthe firing member sequentially engages the staple drivers 7060b to sequentially fire the staples 7070b as the firing member 7056 moves through the second circumferential portion 7045 of the slot 7041.
  • the second circumferential portion 7045 is defined by a constant, or at least substantially constant, radius of curvature about the longitudinal axis 7090; however, other embodiments are envisioned in which the radius of curvature of the second circumferential portion 7045 is not constant.
  • the second circumferential portion 7045 comprises a spiral. Stated another way, in such an instance, the second circumferential portion 7045 recedes away from the longitudinal axis 7090 as it extends around the longitudinal axis 7090.
  • the slot 7041 comprises a transition portion 7044 intermediate the first circumferential portion 7043 and the second circumferential portion 7045.
  • the ramp 7055 slides sequentially through the first circumferential portion 7043, the transition portion 7044, and then the second circumferential portion 7045.
  • the transition portion 7044 permits the firing member 7056 to shift between the first radius of curvature of the first staple row and the second radius of curvature of the second staple row.
  • a transition portion 7044 between the first circumferential portion 7043 and the second circumferential portion 7045 may be unnecessary.
  • first circumferential portion 7043 can comprise a first spiral configuration and the second circumferential portion 7045 can comprise a second spiral configuration which is aligned such that the end of the first spiral configuration is aligned with the beginning of the second spiral configuration, for example.
  • the firing member 7056 is driven along its firing path by a firing drive 7050.
  • the firing drive 7050 is driven about the longitudinal axis 7090 by a handcrank and/or electric motor, for example.
  • the firing drive 7050 comprises a drive recess 7052 defined therein.
  • the base 7054 of the firing member 7056 is positioned in the drive recess 7052.
  • the drive recess 7052 is larger than the base 7054 of the firing member 7056 such that the base 7054 can move, or float, within the drive recess 7052.
  • the drive recess 7052 is defined by sidewalls which limit the movement of the base 7054 within the recess 7052.
  • the firing drive 7050 When the firing drive 7050 is rotated about the longitudinal axis 7090, a sidewall of the drive recess 7052 contacts the base 7054 and pushes the drive member 7056 through the slot 7051.
  • the slot 7051 has one or more changes in its radius of curvature and, when the firing member 7056 moves through such changes, the base 7054 of the firing member 7056 can slide within the drive recess.
  • the staples in the first, or inner, row of staples are deployed sequentially and, then, the staples in the second, or outer, row of staples are deployed sequentially.
  • Such an embodiment can control the inner periphery of the colon before stapling outwardly, for example.
  • the staples in the outer row of staples are deployed sequentially and, then, the staples in the inner row of staples are deployed sequentially.
  • Such an embodiment can establish a boundary in the colon tissue before stapling inwardly, for example.
  • the first staples 7070a and the second staples 7070b have the same unformed height.
  • the first staples 7070a and the second staples 7070b are formed to the same formed height.
  • the first staples 7070a are formed to a first formed height and the second staples 7070b can be formed to a second formed height which is different than the first formed height.
  • the first formed height of the inner row of staples is shorter than the second formed height of the outer row of staples.
  • the first formed height of the inner row of staples is taller than the second formed height of the outer row of staples.
  • Such an arrangement can allow the innermost tissue of a stapled bowel, for example, to be more flexible, for example.
  • first staples 7070a have a first unformed height and the second staples 7070b have a second unformed height which is different than the first unformed height.
  • first staples 7070a and the second staples 7070b are formed to the same formed height.
  • first staples 7070a are formed to a first formed height and the second staples 7070b are formed to a second formed height which is different than the first formed height.
  • the end effector 7000 has two annular rows of staples; however, an end effector can have any suitable number of annular staple rows.
  • an end effector can have three annular rows of staples.
  • the staples in a first annular row can have a first unformed staple height
  • the staples in a second annular row can have a second unformed staple height
  • the third staples in a third annular row can have a third unformed staple height.
  • the staples in a first annular row can have a first deformed staple height
  • the staples in a second annular row can have a second deformed staple height
  • the third staples in a third annular row can have a third deformed staple height.
  • a firing drive 7150 is depicted in FIGS. 100-105 .
  • the firing drive 7150 comprises a rotatable drive shaft 7152 that is rotatable about a longitudinal axis.
  • the firing drive 7150 further comprises a three-stage sequential driver assembly comprising a first, or inner, driver 7154a, a second, or intermediate, driver 7154b, and a third, or outer, driver 7154c.
  • the drive shaft 7152 comprises a drive pin 7151 extending therefrom.
  • the drive pin 7151 extends through a drive slot in each of the drivers 7154a, 7154b, and 7154c.
  • the first driver 7154a comprises a first drive slot 7153a defined therein
  • the second driver 7154b comprises a second drive slot 7153b defined therein
  • the third driver 7154c comprises a third drive slot 7153c defined therein.
  • the drive slots 7153a, 7153b, and 7153c do not have the same configuration; however, the drive slots 7153a, 7153b, and 7153c have overlapping configurations that are aligned, or at least substantially aligned, with each other at the drive pin 7151.
  • the drive pin 7151 is in an unfired position in FIG. 100 and the drive slots 7153a, 7153b, and 7153c are aligned with the drive pin 7151.
  • FIG. 100 illustrates drivers 7154a, 7154b, and 7154c in an unfired position.
  • the drive shaft 7152 is rotated through a first portion of its firing stroke
  • the drive pin 7151 is rotated through a circumferential path where the drive pin 7151 engages a sidewall of the drive slot 7153a and pushes, or cams, the first driver 7154a distally.
  • the drive pin 7151 has not driven the drivers 7154b and 7154c distally during the first portion of the firing stroke.
  • the drive slots 7153b and 7153c are aligned with the circumferential path of the drive pin 7151 throughout the first portion of the firing stroke.
  • the first driver 7154a is configured to fire a first annular row of staples when the first driver 7154a is displaced distally.
  • the drive pin 7151 is rotated through a circumferential path where the drive pin 7151 engages a sidewall of the drive slot 7153b and pushes, or cams, the second driver 7154b distally.
  • the drive pin 7151 has not driven the driver 7154c distally during the second portion of the firing stroke.
  • the drive slots 7153a and 7153c are aligned with the circumferential path of the drive pin 7151 throughout the second portion of the firing stroke.
  • the second driver 7154b is configured to fire a second annular row of staples when the second driver 7154b is displaced distally.
  • the drive pin 7151 is rotated through a circumferential path where the drive pin 7151 engages a sidewall of the drive slot 7153c and pushes, or cams, the third driver 7154c distally. Similar to the above, the drive slots 7153a and 7153b are aligned with the circumferential path of the drive pin 7151 throughout the third portion of the firing stroke.
  • the third driver 7154c is configured to deploy a cutting member when the third driver 7154c is displaced distally; however, in certain embodiments, the third driver 7154c can deploy a third row of staples, for example.
  • first staple firing stage there is no overlap between the first staple firing stage, the second staple firing stage, and the tissue cutting stage. They are timed sequentially. Accordingly, the forces required to deform the staples and cut the tissue are spread out throughout the firing stroke. Moreover, the firing drive 7150 cannot cut the tissue until the tissue has been stapled.
  • first staple firing stage there is some overlap between the first staple firing stage, the second staple firing stage, and/or the tissue cutting stage.
  • the configurations of the drive slots 7153a, 7153b, and 7153c can be adapted such that there is a partial overlap in the movement of the first driver 7154a and the second driver 7154b and/or a partial overlap in the movement of the second driver 7154b and the third driver 7154c.
  • the drivers 7154a, 7154b, and 7154c comprise co-operating features which prevent, or at least inhibit, the drivers 7154a, 7154b, and 7154c from rotating relative to one another.
  • the first driver 7154a comprises a longitudinal key 7155a positioned in a longitudinal slot 7156b defined in the second driver 7154b.
  • the key 7155a and the slot 7156b are configured to permit the first driver 7154a to slide longitudinally relative to the second driver 7154b but block rotational movement between the first driver 7154a and the second driver 7154b.
  • the second driver 7154b comprises a longitudinal key 7155b positioned in a longitudinal slot 7156c defined in the third driver 7154c.
  • the key 7155b and the slot 7156c are configured to permit the second driver 7154b to slide longitudinally relative to the third driver 7154c but block rotational movement between the second driver 7154b and the third driver 7154c.
  • the drive shaft 7152 In order to retract the drivers 7154a, 7154b, and 7154c, the drive shaft 7152 is rotated in an opposite direction. In such instances, the drive shaft 7152 sequentially engages a sidewall of the drive slot 7153c, a sidewall of the drive slot 7153b, and then a sidewall of the drive slot 7153a to return the third driver 7154c, the second driver 7154b, and the first driver 7154a back to their unfired positions ( FIG. 100 ).
  • a firing drive 7250 is illustrated in FIG. 106 .
  • the firing drive 7250 operates in a similar manner to that of the firing drive 7150.
  • the firing drive 7250 comprises a drive shaft 7252 which is rotatable about a longitudinal axis.
  • the drive shaft 7252 comprises a cam surface, or ramp, 7256 which is rotated through several stages of a firing stroke.
  • the firing drive 7250 further comprises a first driver 7254a, a second driver 7254b, and a third driver 7254c which are engaged by the cam 7256 of the drive shaft 7252 when the firing drive 7250 is rotated.
  • the cam 7256 engages a cam surface 7255a defined on the first driver 7254a and drives the first driver 7254a distally.
  • the cam 7256 engages a cam surface 7255b defined on the second driver 7254b and drives the second driver 7254b distally and, in the third stage of the firing stroke, the cam 7256 engages a cam surface 7255c defined on the third driver 7254c and drives the third driver 7254c distally.
  • the first cam surface 7255a is shorter than the second cam surface 7255b and, as a result, the first driver 7254a has a shorter firing stroke than the second driver 7254b.
  • the second cam surface 7255b is shorter than the third cam surface 7255c and, as a result, the second driver 7254b has a shorter firing stroke than the third driver 7254c.
  • the drivers 7254a, 7254b, and 7254c may have any suitable firing stroke.
  • the drivers 7254a, 7254b, and 7254c have the same firing stroke, for example. Such an arrangement may be useful to form different rows of staples to the same formed height, for example.
  • FIG. 107 is a perspective view of a portion of a staple cartridge 4410 for use with a circular surgical stapling instrument in accordance with at least one embodiment.
  • a variety of circular surgical stapling instruments are known.
  • U.S. Patent Application Serial No. 14/836,110, filed August 26, 2015 entitled SURGICAL STAPLING CONFIGURATIONS FOR CURVED AND CIRCULAR STAPLING INSTRUMENTS discloses various circular surgical stapling instrument arrangements.
  • U.S. Patent Application Serial No. 14/498,070, filed September 26,2014 entitled CIRCULAR FASTENER CARTRIDGES FOR APPLYING RADIALLY EXPANDING FASTENER LINES also discloses various circular surgical stapler arrangements.
  • a circular surgical stapler generally comprises a frame assembly that comprises an attachment portion that is configured to operably couple an anvil to the circular surgical stapler.
  • the anvil includes an anvil head that supports an annular line or lines of staple-forming pockets.
  • An anvil stem or trocar portion is attached to the anvil head and is configured to be removably coupled to the anvil attachment portion of the circular stapling instrument.
  • Various circular surgical stapling instruments include means for selectively moving the anvil toward and away from the surgical staple cartridge such that the target tissue may be clamped between the anvil and the deck of the surgical staple cartridge.
  • the surgical staple cartridge removably stores a plurality of surgical staples therein that are arranged in one or more annular arrays that correspond to the arrangement of staple forming pockets provided in the anvil.
  • the staples are removably stored within corresponding staple cavities that are formed in the staple cartridge and are supported on corresponding portions of a selectively movable pusher assembly that is operably received within the circular stapler.
  • the circular stapler further includes an annular knife or cutting member that is configured to incise the tissue that is clamped between the anvil and the staple cartridge.
  • the staple cartridge 4410 comprises a cartridge body 4411 that defines an annular cartridge deck surface 4412.
  • the cartridge body 4411 comprises an inner annular row 4420 of spaced inner staple cavities 4422 and an outer annular row 4440 of spaced outer staple cavities 4442.
  • the inner staple cavities 4422 are staggered relative to the outer spaced staple cavities 4442 as can be seen in FIG. 107 .
  • Supported within each inner staple cavity 4422 is an inner surgical staple 4430 and supported within each outer staple cavity 4442 is an outer surgical staple 4450.
  • the outer staples 4450 in the outer annular row 4440 may have different characteristics than the inner staples 4430 in the inner annular row 4420. For example, as illustrated in the embodiment of FIG.
  • each outer staple 4450 has an unformed "gullwing" configuration.
  • each outer staple 4450 includes a pair of legs 4454, 4464 that extend from a staple crown 4452.
  • Each leg 4454, 4464 includes a vertical portion 4456, 4466, respectively that extends from the crown 4452.
  • the vertical portions 4456,4466 may be parallel to each other in one embodiment. However, in the illustrated arrangement, the vertical portions 4456, 4466 are not parallel to each other.
  • the angle A 1 between the crown 4452 and the vertical portions 4456,4466 in the illustrated arrangement is greater than ninety degrees. See FIG. 108 . Further details regarding the staple configuration may be found in U.S. Patent Application Serial No.
  • At least one leg 4454, 4464 includes an inwardly extending end portion.
  • each leg 4454, 4464 includes an inwardly extending leg portion.
  • leg portion 4458 extends inwardly from the vertical leg portion 4456 and the leg portion 4468 extends inwardly from the vertical leg portion 4466.
  • the leg portion 4458 is shorter than the leg portion 4468. Stated another way, the distance H A between the staple crown 4452 and the point where the leg portion 4458 angles inward from the vertical leg portion 4456 is greater than the distance H C between the staple crown 4452 and the point where the leg portion 4468 angles inward from the vertical leg portion 4466.
  • distance H B in at least one embodiment is shorter than the length H D .
  • the angle A 2 at which the leg portion 4458 angles relative to the vertical leg portion 4556 may be equal to the angle A 3 at which the leg portion 4468 angles relative to the vertical leg portion 4466 or angles A 2 and A 3 may be different from each other. Further details regarding the staple configuration may be found in U.S. Patent Application Serial No. 14/319,008, filed June 30, 2014 , entitled FASTENER CARTRIDGE COMPRISING NON-UNIFORM FASTENERS, U.S. Patent Application Publication No. 2015/0297232 .
  • each inner surgical staple 4430 may have the configuration illustrated in FIG. 108 .
  • the inner surgical staple 4430 has a crown 4432 and two vertical legs 4434,4436 extending therefrom.
  • the vertical legs 4434, 4436 may extend relatively perpendicularly from the crown 4432 or they may extend at angles A 4 that may be greater than ninety degrees. Such arrangement may assist in the temporary retention of the staples 4430 within their corresponding staple cavity 4422.
  • vertical legs 4434, 4436 may extend from the crown 4432 at different angles. In some embodiments, angles A 4 are equal to each other. In other embodiments, angles A 4 are different from each other.
  • the inner staples 4430 and the outer staples 4450 each have the same unformed height UFH.
  • the inner and outer staples 4430, 4450 are formed from conventional surgical staple wire.
  • the diameter of the staple wire used to form the outer staples 4450 is greater than the diameter of the staple wire used to form the inner staples 4430.
  • the inner and outer staples may have the same diameters and be formed from wires with other diameters.
  • the inner and outer staples may be formed from the same type of staple wire. Thus, in such arrangement, the wire diameters of the inner and outer staples would be the same.
  • the inner and outer staples may have the same unformed shapes/configurations, yet be formed from two different staple wires that have different wire diameters.
  • the crown width CWo of each outer staple 4450 is larger than the crown width CW I of each inner staple 4430. Further details regarding the staple configuration may be found in U.S. Patent Application Serial No. 14/319,008, filed June 30, 2014 , entitled FASTENER CARTRIDGE COMPRISING NON-UNIFORM FASTENERS, U.S. Patent Application Publication No. 2015/0297232 .
  • the staple cartridge 4410 includes an outer rim 4414 that extends above the deck surface 4412. During surgery, the clinician can adjust the location of the anvil relative to the cartridge of a circular stapler.
  • the staple cartridge 4410 further comprises deck features 4416 and 4418 that extend from the deck surface 4412. As can be seen in FIG. 107 , a series of inner deck features 4416 are provided between the inner row 4420 of staple cavities 4422 and a centrally-disposed knife opening 4413 through which the knife or cutting member will pass during the firing process.
  • the deck features 4416 may be shaped and located relative to the inner staple cavities and opening 4413 as shown in FIGS. 107, 109 and 110 .
  • each inner deck feature 4416 may have a flat wall portion 4415 that is coextensive with the wall of the knife opening 4413 and a conical or sloping body portion 4417 that is adjacent to the row of inner staple cavities 4422. See FIGS. 109 and 110 .
  • the deck features 4416 are oriented in the gap between two adjacent inner staple cavities 4422 and are staggered between pairs of staple cavities 4422 as shown.
  • the cavity extension arrangements or deck features in this system may serve to lower pressure that is commonly encountered in flat deck cartridges. This disclosed arrangement may also help to mitigate tissue movement and slippage. Since slippage of the tissue is generally undesirable, the outside diameter holding features may be bigger and more numerous.
  • the internal diameter features may serve to increase tissue tension/shear as the blade passes next to the inside internal diameter which may make the system cut better.
  • the deck features 4416 may have different shapes and configurations and may be located in different locations on the deck surface 4412.
  • every other outer staple cavity 4442 includes an outer deck feature 4418 that is associated with each end thereof.
  • Outer deck features 4418 extend above the deck surface 4412 and guide the outer staples 4450 toward the anvil when the staples 4450 are being ejected from the staple cartridge 4410.
  • the outer staples 4450 may not extend above the outer deck features 4418 until they are moved toward the anvil by the firing member.
  • the outer deck features 4418 do not extend around the entirety of the corresponding outer staple cavity 4442.
  • a first outer deck feature 4418 is positioned adjacent a first end of a corresponding outer cavity 4442 and a second outer deck feature 4418 is positioned adjacent a second end of the outer cavity 4442.
  • the outer deck features 4418 are associated with every other one of the outer staple cavities 4442. Such arrangement may serve to lower overall pressure and minimize tissue stretch and movement.
  • first and second outer deck features 4418 may be associated with every one of the outer staple cavities 4442, however.
  • an outer deck feature may extend around the entire perimeter of a corresponding outer cavity.
  • the inner deck features 4416 are shorter than the outer deck features 4418.
  • each inner deck feature protrudes above the deck surface 4412 a distance that is less than the distance that each outer deck feature 4418 protrudes above the deck surface 4412.
  • Each outer deck feature may protrude above the deck surface 4412 the same distance that the outer rim 4414 protrudes above the deck surface 4412.
  • each outer deck feature 4418 has a generally conical or tapered outer profile which may help to prevent tissue from snagging on the deck features during insertion of the stapler head through a patient's colon and rectum.
  • the upstanding outer rim may help to prevent tissue from sliding across the cartridge deck.
  • This upstanding rim could also comprise a repeating pattern of highs and lows rather than being one continuous lip formation.
  • the inside upstanding features may also help to retain the tissue adjacent to the blade and lead to improved cutting.
  • the inside deck features could be between every cavity or in alternative arrangements, the deck feature(s) may comprise one continuous upstanding lip. It may be desirable to balance the number of deck features to minimize the number of high force/compression zones while attaining a desired amount of tissue immobilization.
  • the cavity concentric features may serve the additional purpose of minimization of tissue flow in the areas where the staple legs project from.
  • Such arrangements also facilitate desirable staple formation as the staple legs eject and transition to the receiving anvil pocket which may consist of corresponding forming pockets.
  • Such localized pocket features increase the low compression zones while facilitating leg support from the cartridge as the staple exits the cartridge. This arrangement thereby minimizes the distance that the staple must "jump" before it meets the anvil pocket. Tissue flow tends to increase going from the center of the cartridge radially outward.
  • the improved standing outside row extensions have a tendency to stage tissue as they are inserted up through the colon because it is a tube.
  • FIGS. 109 and 110 illustrate use of the surgical staple cartridge 4410 in connection with an anvil 4480.
  • the anvil 4480 comprises an anvil head portion 4482 that operably supports a staple forming insert or portion 4484 and a knife washer 4490.
  • the knife washer 4490 is supported in confronting relationship to the knife 4492 that is supported in the stapler head.
  • the staple forming insert 4484 is fabricated from, for example, steel, stainless steel, etc. and contains an inner row of inner staple forming pockets 4486 and an outer row of outer staple forming pockets 4488.
  • Each inner staple forming pocket 4486 corresponds to one of the inner staple cavities 4422 and each outer staple forming pocket 4488 corresponds to one of the outer staple cavities 4442.
  • the inner staple forming pockets 4486 are closer to the cartridge deck surface 4412 than are the outer staple forming pockets 4488.
  • the first gap g 1 or first staple forming distance between a first staple forming portion 4485 and the cartridge deck surface 4412 is less than the second gap g 2 or second staple forming distance between a second staple forming portion 4487 and the cartridge deck surface 4412.
  • the inner staples 4430 are each supported within their corresponding inner staple cavity 4422 on a corresponding inner driver portion 4502 of a pusher assembly 4500 and each of the outer staples 4450 are supported within their corresponding outer staple cavity 4442 on a corresponding outer driver portion 4504.
  • Advancement of the pusher assembly 4500 toward the anvil 4480 will cause the inner and outer staples 4430, 4450 to be driven into forming contact with their respective corresponding staple forming pockets 4486, 4488 as shown in FIG. 110 .
  • the knife 4492 is advanced distally through the tissue that is clamped between the anvil 4480 and the deck surface 4412 and through a frangible bottom 4491 of the knife washer 4490.
  • Such arrangement serves to provide the outer staples 4450 with a formed height FH O that is larger than the formed height FH I of the inner staples 4430.
  • the outer row 4440 of outer staples 4450 are formed into a larger "B" formation resulting in a greater capture volume and/or taller staple forming height to alleviate high tissue compression near the outer row of staples 4440.
  • a larger B formation may also improve blood flow toward the inner rows.
  • the outer row 4440 of outer staples 4450 comprise a greater resistance to unfolding by utilizing a larger staple crown, staple leg widths, and/or staple leg thicknesses.
  • the quantity of staples used in each row of staples can vary. In one embodiment, for example, there are more outer staples 4450 than there are inner staples 4430. Another embodiment employs more inner staples 4430 than outer staples 4450. In various instances, the wire diameter of the outer staples 4450 is larger than the wire diameter of the inner staples 4430.
  • the inner and outer staples 4430, 4450 may have the same unformed heights UFH.
  • the crown widths CW O in the outer row 4440 of outer staples 4450 are larger than the crown widths CW I of the inner row 4420 of inner staples 4430.
  • the gullwing configuration of the outer staples 4450 employs bends that are located at different distances from their respective crown. Use of the stepped anvil configuration with a flat (unstepped) cartridge deck surface 4412 with uniform driver or pusher travel yield staples with different formed heights.
  • FIG. 111 illustrates another staple cartridge embodiment 4610.
  • the staple cartridge 4610 includes a cartridge deck 4612 that includes an inner annular row 4620 of spaced inner staple cavities 4622 and an outer annular row 4640 of outer spaced staple cavities 4642.
  • the inner staple cavities 4622 are staggered relative to the outer spaced staple cavities 4642 as can be seen in FIG. 111 .
  • Supported within each inner staple cavity 4622 is an inner surgical staple 4630 and supported within each outer staple cavity 4642 is an outer surgical staple 4650.
  • an outer rim 4614 extends above the deck surface 4612.
  • the staples 4630, 4650 do not protrude above the deck surface 4612 until they are moved toward the anvil by the firing member. Such embodiments may frequently utilize small staples relative to the depth of their respective staple cavity in which they are stored. In other embodiments, the legs of the staples protrude above the deck surface 4612 when the staples are in their unfired positions.
  • the staple cartridge 4610 further comprises deck features 4616 and 4618 that extend from the deck surface 4612.
  • every other inner staple cavity 4622 includes an inner deck feature 4616 that is associated with each end thereof.
  • Inner deck features 4616 extend above the deck surface 4612 and guide the corresponding inner staples 4630 toward the anvil when the corresponding inner staples 4630 are being ejected from the staple cartridge 4610.
  • the inner staples 4630 may not extend above the inner deck features 4616 until they are moved toward the anvil by the firing member.
  • the inner deck features 4616 do not extend around the entirety of the corresponding inner staple cavity 4622.
  • a first inner deck feature 4616 is positioned adjacent a first end of a corresponding inner cavity 4622 and a second inner deck feature 4616 is positioned adjacent a second end of the inner cavity 4622.
  • the inner deck features 4416 may be associated with every one of the inner staple cavities 4622, however.
  • an inner deck feature may extend around the entire perimeter of a corresponding inner staple cavity.
  • each outer staple cavity 4642 includes an outer deck feature 4618 that is associated with each end thereof.
  • Outer deck features 4618 extend above the deck surface 4612 and guide the outer staples 4650 toward the anvil when the staples 4650 are being ejected from the staple cartridge 4610.
  • the outer staples 4650 may not extend above the outer deck features 4618 until they are moved toward the anvil by the firing member.
  • the outer deck features 4618 do not extend around the entirety of the corresponding outer staple cavity 4642.
  • a first outer deck feature 4618 is positioned adjacent a first end of a corresponding outer cavity 4642 and a second outer deck feature 4618 is positioned adjacent a second end of the outer cavity 4642.
  • outer deck features 4618 are associated with every one of the outer staple cavities 4642.
  • first and second outer deck features 4618 may be associated with every other one of the outer staple cavities 4642, however.
  • an outer deck feature may extend around the entire perimeter of a corresponding outer cavity.
  • the inner deck features 4616 and the outer deck features 4618 extend above the deck surface 4612 the same distance. Stated another way, they have the same heights.
  • each inner deck feature 4416 and each outer deck feature 4618 has a generally conical or tapered outer profile which may help to prevent tissue from snagging on the deck features during insertion of the stapler head through a patient's colon and rectum.
  • FIGS. 112 and 113 illustrate use of the surgical staple cartridge 4610 in connection with an anvil 4680.
  • the anvil 4680 comprises an anvil head portion 4682 that operably supports a staple forming insert or portion 4684 and a knife washer 4690.
  • the knife washer 4690 is supported in confronting relationship to a knife 4692 that is supported in the stapler head.
  • the staple forming insert 4684 is fabricated from, for example, steel, stainless steel, etc. and contains an inner row of inner staple forming pockets 4686 and an outer row of outer staple forming pockets 4688.
  • Each inner staple forming pocket 4686 corresponds to one of the inner staple cavities 4622 and each outer staple forming pocket 4688 corresponds to one of the outer staple cavities 4642.
  • the inner staple forming pockets 4686 are located the same distance g 1 from the deck surface 4612 as are the outer staple forming pockets 4688.
  • an inner staple 4630 is supported within a corresponding inner staple cavity 4622 on a corresponding inner driver portion 4702 of a pusher assembly 4700.
  • An outer staple 4650 is supported within a corresponding outer staple cavity 4642 on a corresponding outer driver portion 4704. Advancement of the pusher assembly 4700 toward the anvil 4680 will cause the inner and outer staples 4630,4650 to be driven into forming contact with their respective corresponding staple forming pockets 4686, 4688 as shown in FIG. 113 .
  • the knife 4692 is advanced distally through the tissue that is clamped between the anvil 4680 and the deck surface 4612 and through a frangible bottom 4691 of the knife washer 4690.
  • each inner staple 4630 is formed from a first staple wire that has a first wire diameter D 1 and has a first unformed height L 1 .
  • the first wire diameter D 1 may be approximately 0,201 mm - 0,381 mm (approximately 0.0079" - 0.015") (increments are usually 0,226 mm, 0,239 mm, and 0,037 mm (0.0089", 0.0094", and 0.00145”)) and the first unformed height L 1 may be approximately 5,023 mm - 6,350 mm (approximately 0.198" - 0.250”) .
  • Each outer staple 4650 is formed from a second staple wire that has a second wire diameter D 2 and has a second unformed height L 2 .
  • D 1 ⁇ D 2 and L 1 ⁇ L 2 are formed with the same formed heights FH's.
  • the thicker wire staples on the outside tend to provide high tear and burst strengths as compared to the inside row of smaller diameter staples which tend to hold better hemostatically. Stated another way, the tighter inside rows of staples may hold better hemostatically while the outer rows of less compressed staples may facilitate better healing and blood flow.
  • the staples with longer legs even when formed at the same heights as staples with shorter legs, may ensure more B-bending which may make the longer legged staples stronger and more likely to be properly formed enough to hold in high load conditions.
  • the quantity of staples used in each row of staples can vary.
  • the inner row 4620 has the same number of inner staples 4630 as does the outer row 4640 of outer staples 4650.
  • the crown widths of the staples 4650 is larger than the crown widths of the inner staples 4630.
  • the staples 4630, 4650 may have identical crown widths.
  • the staples 4630, 4650 may be of the gullwing design described above.
  • At least one leg of the staple may include an end portion that is bent inwardly or both legs may include end portions that are bent inwardly toward each other.
  • Such staples may be employed in the inner annular row or the outer annular row or in both of the inner and outer annular rows.
  • FIG. 114 illustrates another circular staple cartridge embodiment 4810 that includes a cartridge deck 4812 that includes three annular rows 4820, 4840, 4860 of spaced staple cavities.
  • the inner or first row 4820 contains a first plurality of inner or first staple cavities 4822 that are each arranged at a first angle.
  • Each inner staple cavity 4822 operably supports a corresponding inner or first staple 4830 therein.
  • the inner cavities 4822 orient the first staples 4830 at the same uniform angle relative to the tangential direction.
  • each inner staple 4830 is formed from a first staple wire that has a first staple diameter D 1 .
  • each inner staple 4830 includes a first crown 4832 and two first legs 4834.
  • the first crown has a first crown width C 1 and each first leg 4834 has a first unformed leg length L 1 .
  • the first crown width C 1 may be approximately 2,540 mm - 7,620 mm (approximately 0.100" - 0.300") and the first unformed leg length L 1 may be approximately 5,023 mm - 6,350 mm (approximately 0.198" - 0.250”) .
  • the first legs 4834 may be each arranged at an angle A 1 relative to the first staple crown 4832.
  • the angle A 1 may be approximately 90° or it may be slightly greater than 90° such that the first legs 4834 are slightly splayed outward to assist in retaining the first staple 4830 in its corresponding first staple cavity 4822.
  • the staple cartridge 4810 is intended to be used in connection with an anvil 4900 that includes two inner or first rows 4902 of staggered or angled first pairs 4903 of first staple forming pockets 4904. Each first pair 4903 of first staple forming pockets 4904 correspond to one first staple 4830. One first staple forming pocket 4904 corresponds to one first staple leg 4834 and the other first staple forming pocket 4904 of the pair 4903 corresponds to the other first staple leg 4834.
  • Such arrangement serves to establish a formed staple configuration wherein the first staple legs 4834 of a first staple 4830 are formed out of plane with the first crown 4832 of that particular first staple 4830 such that one first leg 4834 is formed on one side of the first crown 4832 and the other first leg 4834 is formed on the other side of the first crown 4832.
  • This "three-dimensional" formed staple configuration is shown with respect to some of the first staple forming pockets 4904 in FIG. 115 .
  • the cartridge deck 4812 is of "stepped" construction.
  • the cartridge deck 4812 includes an inner or first cartridge deck portion 4814 that corresponds to the inner or first annular row 4820 of inner or first staple cavities 4822.
  • the portion of the anvil 4900 containing the first staple forming pockets 4904 is spaced from the deck portion 4814 a first gap distance g 1 .
  • the middle or second row 4840 contains a second plurality of middle or second staple cavities 4842 that are each arranged at a second angle.
  • Each middle staple cavity 4842 operably supports a corresponding middle or second staple 4850 therein.
  • the middle cavities 4842 orient the middle or second staples 4850 at the same uniform second angle relative to the tangential direction. However, the second angle differs from the first angle. Stated another way, when the first and second staples are supported in their respective first and second cavities, the axis of the first crown of each first staple 4830, when extended, would ultimately intersect the extended axis of the second crown of an adjacent second staple 4850. As can be seen in FIGS.
  • each second or middle staple 4850 comprises a second staple crown or base 4852 and two second legs 4854.
  • the staple base 4852 may have a somewhat rectangular cross-sectional shape and be formed from a flat sheet of material.
  • the second staple legs 4854 may have a round cross-sectional profile, for example.
  • the second or middle staples may comprise various staple configurations disclosed in, for example, U.S. Patent Application Serial No. 14/836,110, filed August 26, 2015 , entitled SURGICAL STAPLING CONFIGURATIONS FOR CURVED AND CIRCULAR STAPLING INSTRUMENTS. Having round staple legs that extend from a staple base portion having the rectangular cross-sectional profile can provide a staple base portion and staple legs with no preferential bending planes.
  • the second staple 4850 comprises bend portions 4856 where the staple legs 4854 extend from the staple base portion 4852.
  • the bend portions 4856 may comprise a substantially square cross-sectional profile.
  • the square profile and the rectangular profile of the bend portions 4856 and the staple base portion 4852, respectively, provide a stiff connection and backbone to the round staple legs 4854.
  • the round staple legs 4854 eliminate preferential bending planes that staple legs with a square, rectangular, or any shape with vertices or a non-uniform shape, cross-sections could have.
  • Each of the second staple legs 4854 has a second diameter D 2 . In at least one embodiment, D 2 > D 1 .
  • the second base or crown 4852 has a second crown width C 2 . In one arrangement, C 2 > C 1 .
  • the second legs 4854 may be each arranged at an angle A 2 relative to the second base or crown 4852.
  • the angle A 2 may be approximately 90° or it may be slightly greater than 90° such that the second legs 4854 are slightly splayed outward to assist in retaining the second staple 4850 in its corresponding second staple cavity 4842.
  • the anvil 4900 further comprises two middle or second rows 4912 of staggered or angled second pairs 4913 of second staple forming pockets 4914.
  • Each second pair 4913 of second staple forming pockets 4914 correspond to one second staple 4850.
  • One second staple forming pocket 4914 corresponds to one second staple leg 4854 and the other second staple forming pocket 4914 of the pair 4913 corresponds to the other second staple leg 4854.
  • Such arrangement serves to establish a formed staple configuration wherein the second legs 4854 are formed out of plane with the second base 4852 of the particular second staple 4850.
  • This "three-dimensional" formed staple configuration is shown with respect to some of the second staple forming pockets 4914 in FIG. 115 .
  • the cartridge deck 4812 further comprises a second cartridge deck portion 4816 that corresponds to the middle or second annular row 4840 of middle or second staple cavities 4842.
  • the portion of the anvil 4900 containing the second staple forming pockets 4914 is spaced from the deck portion 4816 a second gap distance g 2 .
  • g 2 > g 1 .
  • the outside or third row 4860 contains a third plurality of outside or third staple cavities 4862 that are sized relative to the second staple cavities 4842 such that each outer or third staple cavity 4862 spans a distance between two adjacent second cavities 4842.
  • Each outer staple cavity 4862 operably supports a corresponding outer or third staple 4870 therein.
  • the outer cavities 4862 orient the outer or third staples 4870 tangent to the circumferential direction.
  • each third or outer staple 4870 comprises a third staple crown or base 4872 and two third legs 4874.
  • the staple base 4872 may have a somewhat rectangular cross-sectional shape and be formed from a flat sheet of material.
  • the third staple legs 4874 may have a round cross-sectional profile, for example.
  • the third or outer staples 4870 may comprise various staple configurations disclosed in, for example, U.S. Patent Application Serial No. 14/836,110, filed August 26, 2015 , entitled SURGICAL STAPLING CONFIGURATIONS FOR CURVED AND CIRCULAR STAPLING IN. Having round staple legs that extend from a staple base portion having the rectangular cross-sectional profile can provide a staple base portion and staple legs with no preferential bending planes.
  • the third staple 4870 comprises bend portions 4876 where the staple legs 4874 extend from the staple base portion 4872.
  • the bend portions 4876 may comprise a substantially square cross-sectional profile.
  • the square profile and the rectangular profile of the bend portions 4876 and the staple base portion 4872, respectively, provide a stiff connection and backbone to the round staple legs 4874.
  • the round staple legs 4874 eliminate preferential bending planes that staple legs with a square, rectangular, or any shape with vertices or a non-uniform shape, cross-sections could have.
  • the third base or crown 4872 has a third crown width C 3 and each third leg 4874 has a third unformed leg length L 3.
  • the third legs 4874 may be each arranged at an angle A 3 relative to the third base or crown 4872.
  • the angle A 3 may be approximately 90° or it may be slightly greater than 90° such that the third legs 4874 are slightly splayed outward to assist in retaining the third staple 4870 in its corresponding third staple cavity 4862.
  • the anvil 4900 further comprises an outer row 4916 of outer or third staple forming pockets 4918.
  • Each third staple forming pocket 4918 corresponds to one third staple 4870.
  • the cartridge deck 4812 further comprises a third cartridge deck portion 4818 that corresponds to the outer or third row 4860 of outer or third staple cavities 4862.
  • the portion of the anvil 4900 containing the third staple forming pockets 4918 is spaced from the deck portion 4818 a third gap distance g 3. In the illustrated example, g 3 > g 2 .
  • FIG. g 3 > g 2 .
  • a tissue thickness compensator 4920 is employed in connection with each outer or third staple 4870.
  • the tissue thickness compensator may comprise a woven material that is embedded with oxidized regenerated cellulose (ORC) to promote hemostasis.
  • the tissue thickness compensator 4920 may comprise any of the various tissue thickness compensator arrangements disclosed in U.S. Patent Application Serial No. 14/187,389, filed February 24, 2014 , entitled IMPLANTABLE LAYER ASSEMBLIES, U.S. Patent Application Publication No. 2015/0238187 .
  • the tissue thickness compensator 4920 has a thickness designated as "a".
  • the tissue thickness compensator has a thickness of approximately 0.015" - 0.045". However, other thicknesses may be employed.
  • the staple cartridge 4810 may employ a different number of staples in each of the three rows of staples.
  • the inner row of staples comprises conventional staples with the smallest wire diameter and the shortest unformed leg length.
  • Each first staple has the shortest crown width and each first staple is oriented at a uniform angle relative to the tangential direction.
  • the middle staples have a configuration that differs from the first staple configuration.
  • Each leg of the middle staples comprises a moderate wire diameter and unformed leg length.
  • Each middle staple has a slightly larger crown width than the crown widths of the inner staples and each middle staple is oriented at a uniform angle relative to the tangential direction, but at a different angle relative to the inner row of inner staples.
  • Each outer staple has a configuration that is similar to the configuration of the middle staples.
  • Each of the third legs of each outer staple comprises the largest wire diameter as compared to the wire diameters of the legs of the inner and middle staples.
  • the crown width of each outer staple is significantly larger than the crown widths of the inner and middle staples.
  • Each outer staple is oriented tangentially to the circumferential direction of the cartridge.
  • the outer row of staples employs woven tissue thickness compensators (spacer fabric) that is embedded with ORC to promote hemostasis.
  • the stepped anvil and the stepped cartridge deck yield different formed staple heights with the staples having the shortest formed heights being in the inner row and the staples having the longest formed heights being in the outer row.
  • the anvil pockets corresponding to the inner and middle rows of staples are "tilted” to create three dimensional staples in the inner and middle rows.
  • "Bathtub-type" anvil pockets correspond to the outer row of staples.
  • the staples may be sequentially fired. For example, the staples in the inner and middle rows may be fired first and the staples in the outer row fired thereafter.
  • the annular knife cuts the clamped tissue during the firing process.
  • a circular stapling instrument includes an anvil and a staple cartridge.
  • One or both of the anvil and the staple cartridge is movable relative to the other between an open configuration and a closed configuration to capture tissue therebetween.
  • the staple cartridge houses staples inside, or at least partially inside, circular rows of staple cavities.
  • the staples are deployed in circular rows from their respective staple cavities into the captured tissue and are formed against corresponding circular rows of forming pockets in the anvil.
  • a firing drive is configured to eject the staples from the staple cartridge during a firing stroke of the firing drive.
  • An anvil of a circular stapling instrument generally comprises a tissue compression surface and an annular array of staple forming pockets defined in the tissue compression surface.
  • the anvil further comprises an attachment mount and a stem extending from the attachment mount.
  • the stem is configured to be releasably attached to a closure drive of the circular stapling instrument so that the anvil can be moved toward and away from a staple cartridge of the circular stapling instrument.
  • the staple cartridge and the anvil can travel separately within a patient and are combined at the surgical field.
  • the staple cartridge for example, travels through a narrow tubular body of the patient such as, for example, a colon.
  • a staple cartridge may include several tissue-contacting features such as, for example, stepped decks and pocket extenders. To avoid unintentional injury to the patient as the staple cartridge travels toward a target tissue, the present disclosure, among other things, presents various modifications to several tissue-contacting features.
  • a partial cross-sectional view depicts a staple cartridge 15500 of a circular surgical instrument pressing against tissue (T) as the staple cartridge 15500 travels within a patient's body.
  • Multiple structural features of the staple cartridge 15500 are modified to create an especially contoured outer frame 15502 to protect the tissue.
  • the staple cartridge 15500 includes a plurality of annular rows of staple cavities.
  • an outer row 15504 of staple cavities 15510 at least partially surrounds an inner row 15506 of staple cavities 15512, as illustrated in FIG. 118 .
  • the staple cavities 15510 and 15512 are configured to house staples 15530 and 15531, respectively.
  • inner and outer delineate a relationship with reference to a central axis 15533.
  • an inner tissue-contacting surface 15518 is closer to the central axis 15533 than outer tissue-contacting surface 15516.
  • the staple cartridge 15500 comprises a stepped cartridge deck 15508.
  • the outer row 15504 is defined in an outer tissue-contacting surface 15516 of the stepped cartridge deck 15508 while the inner row 15506 is defined in an inner tissue-contacting surface 15518 of the stepped cartridge deck 15508.
  • the outer tissue-contacting surface 15516 is stepped down from the inner tissue-contacting surface 15518 which creates a gradient that reduces friction as the staple cartridge 15500 is pressed against the tissue.
  • the outer tissue-contacting surface 15516 is parallel, or at least substantially parallel, to the inner tissue-contacting surface 15518. In other instances, the outer tissue-contacting surface 15516 is slanted such that a first plane defined by the outer tissue-contacting surface 15516 is transverse to a second plane defined by the inner tissue-contacting surface 15518.
  • An angle is defined between the first plane and the second plane. The angle can be an acute angle. In at least one instance, the angle can be any angle selected from a range of greater than about 0° and less than or equal to about 30°, for example. In at least one instance, the angle can be any angle selected from a range of greater than about 5° and less than or equal to about 25°, for example.
  • the angle can be any angle selected from a range of greater than about 10° and less than or equal to about 20°, for example.
  • a slanted outer tissue-contacting surface 15516 can reduce friction against, or snagging of, tissue as the staple cartridge 15500 is moved relative to the tissue.
  • a slanted outer tissue-contacting surface 15516 is also stepped down from the inner tissue-contacting surface 15518.
  • an inner portion of the outer tissue-contacting surface 15516 is planar, or at least substantially planar while an outer edge 15548 of the outer tissue-contacting surface 15516 is pitched, radiused, and/or beveled to reduce friction against, or snagging of, tissue as the staple cartridge 15500 is moved relative to the tissue.
  • the staple cavities 15510 reside in the planar inner portion of the outer tissue-contacting surface 15516, for example.
  • An outer edge 15550 of the inner tissue-contacting surface 15518 can also be pitched, beveled and/or radiused to reduce friction against, or snagging of, tissue as the staple cartridge 15500 is moved relative to the tissue.
  • the staple cavities 15510 of the outer row 15504 comprise pocket extenders 15514.
  • the pocket extenders 15514 are configured to control and guide the staples 15530 as they are ejected from their respective staple cavities 15510.
  • the pocket extenders 15514 can be configured to accommodate staples with a greater unformed height s that the staples of the inner tissue-contacting surface 15518, for example.
  • a staple cavity 15510 in the outer row 15504 is laterally aligned, or at least substantially aligned, with a gap 15520 between two adjacent staple cavities 15512 in the inner row 15506.
  • the staple cavity 15510 includes a first end 15522 and a second end 15524.
  • the second end 15524 overlaps with a first end 15526 of one of the two consecutive staple cavities 15512 such that a staple leg 15530a positioned at the second end 15524 is radially aligned, or at least substantially aligned, with a staple leg 15531a positioned at the first end 15526, as illustrated in FIG. 118 .
  • the first end 15522 of the staple cavity 15510 overlaps with a second end 15528 of the other one of the two consecutive staple cavities 15512.
  • a pocket extender 15514 comprises a first jacket 15532 protruding from the outer tissue-contacting surface 15516 to conceal a tip 15536 of the staple leg 15530a that extends beyond the outer tissue-contacting surface 15516.
  • the first jacket 15532 comprises an end 15538 protruding from the first end 15522, an inner side wall 15540 and an outer side wall 15542 extending away from the end 15538 to form the first jacket 15532.
  • the first jacket 15532 defines, or at least substantially defines, a "C" shaped wall extending on a portion of a perimeter 15535 of the staple cavity 15510 that comprises the first end 15522.
  • the inner side wall 15540 protrudes from the outer tissue-contacting surface 15516 to a greater height than the outer side wall 15542. Said another way, the outer side wall 15542 is lower in height than the inner side wall 15540.
  • This arrangement creates a gradient for a smooth transition from the inner side wall 15540 to the outer side wall 15542 to the outer tissue-contacting surface 15516.
  • the inner side wall 15540 and the inner tissue-contacting surface 15518 comprise the same, or at least substantially the same, height with reference to the outer tissue-contacting surface 15516.
  • the inner side wall 15540 and the inner tissue-contacting surface 15518 comprise different heights with reference to the outer tissue-contacting surface 15516.
  • the inner side wall 15540 is lower in height relative to the inner tissue-contacting surface 15518 with reference to the outer tissue-contacting surface 15516. This arrangement creates a gradient for a smooth transition from the inner tissue-contacting surface 15518 to the inner side wall 15540 to the outer side wall 15542 to the outer tissue-contacting surface 15516.
  • the inner tissue-contacting surface 15518, the inner side wall 15540, the outer side wall 15542, and/or the outer tissue-contacting surface 15516 define discrete portions of the contoured outer frame 15502; nonetheless, as illustrated in FIG. 118 , such portions are kept sufficiently close to one another so that tissue cannot be trapped therebetween as the staple cartridge 15500 presses against the tissue. Furthermore, one or more of the portions may include slanted, contoured, curved, radiused, and/or beveled outer surfaces to reduce friction against the tissue. As illustrated in FIG.
  • an upper surface 15544 of the outer side wall 15542 and an upper surface 15546 of the inner side wall 15540 are slanted, contoured, curved, radiused, and/or beveled to define the contoured outer frame 15502.
  • the upper surface 15544 and the upper surface 15546 define a slanted plane that is transverse to a first plane defined by the outer tissue-contacting surface 15516 and a second plane defined by the inner tissue-contacting surface 15518.
  • a first angle is defined between the slanted plane and the first plane.
  • a second angle can also be defined between the slanted plane and the second plane.
  • the first and second angles can be the same, or at least substantially the same in value. Alternatively, the first angle can be different from the second angle in value.
  • the first angle and/or the second angle are acute angles.
  • the first angle is any angle selected from a range of greater than about 0° and less than or equal to about 30°, for example. In at least one instance, the first angle is any angle selected from a range of greater than about 5° and less than or equal to about 25°, for example. In at least one instance, the first angle is any angle selected from a range of greater than about 10° and less than or equal to about 20°, for example. In at least one instance, the second angle is any angle selected from a range of greater than about 0° and less than or equal to about 30°, for example. In at least one instance, the second angle is any angle selected from a range of greater than about 5° and less than or equal to about 25°, for example. In at least one instance, the second angle is any angle selected from a range of greater than about 10° and less than or equal to about 20°, for example.
  • the pocket extender 15514 includes a second jacket 15534 that is similar in many respects to the first jacket 15532. Like the first jacket 15532, the second jacket 15534 protrudes from the outer tissue-contacting surface 15516 to conceal a tip of a staple leg that extends beyond the outer tissue-contacting surface 15516.
  • the second jacket 15534 comprises an end 15538 protruding from the second end 15524, an inner side wall 15540 and an outer side wall 15542 extending from the end 15538 to form the second jacket 15534.
  • pocket extender 15514 is illustrated in FIG. 119 , it is understood that one or more other pocket extenders 15514 may protrude from the outer tissue-contacting surface 15516, for example.
  • first jacket 15532 and the second jacket 15534 are connected via side walls to define a pocket extender that completely surrounds a staple cavity, for example.
  • FIG. 82A schematically depicts a robotic surgical instrument system 20'; however, U.S. Patent Application Serial No. 13/118,241 , entitled SURGICAL STAPLING INSTRUMENTS WITH ROTATABLE STAPLE DEPLOYMENT ARRANGEMENTS, now U.S. Patent Application Publication No. 2012/0298719 , for example, discloses several examples of a robotic surgical instrument system in greater detail.
  • an end effector in accordance with various embodiments can comprise electrodes configured to heat and seal the tissue.
  • an end effector in accordance with certain embodiments can apply vibrational energy to seal the tissue.
  • the devices disclosed herein can be designed to be disposed of after a single use, or they can be designed to be used multiple times. In either case, however, a device can be reconditioned for reuse after at least one use. Reconditioning can include any combination of the steps including, but not limited to, the disassembly of the device, followed by cleaning or replacement of particular pieces of the device, and subsequent reassembly of the device. In particular, a reconditioning facility and/or surgical team can disassemble a device and, after cleaning and/or replacing particular parts of the device, the device can be reassembled for subsequent use.
  • reconditioning of a device can utilize a variety of techniques for disassembly, cleaning/replacement, and reassembly. Use of such techniques, and the resulting reconditioned device, are all within the scope of the present application.
  • the devices disclosed herein may be processed before surgery.
  • a new or used instrument may be obtained and, when necessary, cleaned.
  • the instrument may then be sterilized.
  • the instrument is placed in a closed and sealed container, such as a plastic or TYVEK bag.
  • the container and instrument may then be placed in a field of radiation that can penetrate the container, such as gamma radiation, x-rays, and/or high-energy electrons.
  • the radiation may kill bacteria on the instrument and in the container.
  • the sterilized instrument may then be stored in the sterile container.
  • the sealed container may keep the instrument sterile until it is opened in a medical facility.
  • a device may also be sterilized using any other technique known in the art, including but not limited to beta radiation, gamma radiation, ethylene oxide, plasma peroxide, and/or steam.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Surgical Instruments (AREA)

Claims (10)

  1. Ensemble outil interchangeable, comprenant :
    un logement ;
    une entrée d'entraînement rotatif (2418) ; et
    un effecteur terminal (2200), comprenant :
    un premier arbre de sortie rotatif (2440) ;
    un second arbre de sortie rotatif (2530) ; et
    une transmission (2420) configurable dans trois états de fonctionnement :
    un premier état de fonctionnement dans lequel ladite entrée d'entraînement est accouplée fonctionnellement avec ledit premier arbre de sortie rotatif et fonctionnellement désolidarisée dudit second arbre de sortie rotatif ;
    un deuxième état de fonctionnement dans lequel ladite entrée d'entraînement est accouplée fonctionnellement avec ledit second arbre de sortie rotatif et fonctionnellement désolidarisée dudit premier arbre de sortie rotatif ; et
    un troisième état de fonctionnement dans lequel ladite entrée d'entraînement est accouplée fonctionnellement avec ledit premier arbre de sortie rotatif et ledit second arbre de sortie rotatif.
  2. Ensemble outil interchangeable selon la revendication 1, dans lequel ledit effecteur terminal comprend en outre une cartouche d'agrafes comprenant des agrafes stockées de manière amovible en son sein, et dans lequel ledit premier arbre de sortie rotatif fait partie d'un système de déclenchement d'agrafes conçu pour éjecter lesdites agrafes de ladite cartouche d'agrafes.
  3. Outil interchangeable selon la revendication 2, dans lequel ledit effecteur terminal comprend en outre un élément de coupe conçu pour inciser un tissu capturé à l'intérieur dudit effecteur terminal, et dans lequel ledit second arbre de sortie rotatif est en prise fonctionnelle avec ledit élément de coupe.
  4. Ensemble outil interchangeable selon la revendication 2 ou la revendication 3, dans lequel ledit effecteur terminal comprend en outre une enclume conçue pour déformer lesdites agrafes, et dans lequel ledit second arbre de sortie rotatif fait partie d'un système de fermeture conçu pour déplacer ladite enclume entre une position ouverte et une position fermée.
  5. Ensemble outil interchangeable selon l'une quelconque des revendications 1 à 4, dans lequel ledit effecteur terminal comprend en outre un élément de coupe conçu pour inciser un tissu capturé à l'intérieur dudit effecteur terminal, et dans lequel ledit premier arbre de sortie rotatif est en prise fonctionnelle avec ledit élément de coupe.
  6. Outil interchangeable selon la revendication 5, dans lequel ledit effecteur terminal comprend en outre une cartouche d'agrafes comprenant des agrafes stockées de manière amovible en son sein et une enclume conçue pour déformer lesdites agrafes, et dans lequel ledit second arbre de sortie rotatif fait partie d'un système de fermeture conçu pour déplacer ladite enclume entre une position ouverte et une position fermée.
  7. Système d'instrument d'agrafage, comprenant :
    un instrument comprenant une poignée et une sortie ; et
    un ensemble outil interchangeable selon l'une quelconque des revendications 1 à 6 pouvant être fixé audit instrument, dans lequel l'entrée d'entraînement rotatif est en prise fonctionnelle avec ladite sortie.
  8. Ensemble outil interchangeable selon l'une quelconque des revendications 1 à 6, ou système d'instrument d'agrafage selon la revendication 7, dans lequel ledit effecteur terminal comprend une structure, dans lequel ladite transmission comprend un actionneur à entraînement électrique monté sur ladite structure.
  9. Ensemble outil interchangeable selon l'une quelconque des revendications 1 à 6 et 8, ou système d'instrument d'agrafage selon la revendication 7 ou la revendication 8, dans lequel ledit premier arbre de sortie rotatif et ledit second arbre de sortie rotatif sont coaxiaux.
  10. Ensemble outil interchangeable selon la revendication 1, dans lequel la transmission comprend une bascule à actionnement électrique.
EP17164412.3A 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un mécanisme de transmission réglable Active EP3225185B1 (fr)

Applications Claiming Priority (15)

Application Number Priority Date Filing Date Title
US15/089,210 US10478190B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a spent cartridge lockout
US15/089,284 US20170281186A1 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a contourable shaft
US15/089,349 US10682136B2 (en) 2016-04-01 2016-04-01 Circular stapling system comprising load control
US15/089,258 US10342543B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a shiftable transmission
US15/089,336 US10709446B2 (en) 2016-04-01 2016-04-01 Staple cartridges with atraumatic features
US15/089,321 US10271851B2 (en) 2016-04-01 2016-04-01 Modular surgical stapling system comprising a display
US15/089,203 US10542991B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a jaw attachment lockout
US15/089,326 US10433849B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a display including a re-orientable display field
US15/089,309 US10675021B2 (en) 2016-04-01 2016-04-01 Circular stapling system comprising rotary firing system
US15/089,325 US11045191B2 (en) 2016-04-01 2016-04-01 Method for operating a surgical stapling system
US15/089,278 US10420552B2 (en) 2016-04-01 2016-04-01 Surgical stapling system configured to provide selective cutting of tissue
US15/089,300 US10456140B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising an unclamping lockout
US15/089,196 US10568632B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a jaw closure lockout
US15/089,295 US10856867B2 (en) 2016-04-01 2016-04-01 Surgical stapling system comprising a tissue compression lockout
US15/089,312 US11284890B2 (en) 2016-04-01 2016-04-01 Circular stapling system comprising an incisable tissue support

Publications (3)

Publication Number Publication Date
EP3225185A2 EP3225185A2 (fr) 2017-10-04
EP3225185A3 EP3225185A3 (fr) 2018-07-11
EP3225185B1 true EP3225185B1 (fr) 2020-10-14

Family

ID=68069424

Family Applications (23)

Application Number Title Priority Date Filing Date
EP17164408.1A Active EP3225184B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant un système de déclenchement rotatif
EP20150529.4A Active EP3656315B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant une mâchoire de blocage de fermeture
EP17164412.3A Active EP3225185B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un mécanisme de transmission réglable
EP17164433.9A Active EP3238639B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical conçu pour réaliser une coupe sélective de tissus
EP21214545.2A Pending EP3988035A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de cartouche usagée
EP19203275.3A Pending EP3616630A1 (fr) 2016-04-01 2017-03-31 Cartouches d'agrafes ayant des éléments atraumatiques
EP18208037.4A Pending EP3461424A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical modulaire comprenant un dispositif d'affichage
EP17164294.5A Active EP3225194B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de compression de tissu
EP20176510.4A Pending EP3718487A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un écran incluant un champ d'affichage ré-orientable
EP23199750.3A Pending EP4275626A3 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant une commande de charge
EP17164088.1A Active EP3225176B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical modulaire comprenant un dispositif d'affichage
EP19217086.8A Pending EP3656316A3 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de fixation de mâchoire
EP17164406.5A Active EP3225198B1 (fr) 2016-04-01 2017-03-31 Cartouches d'agrafes ayant des caractéristiques atraumatiques
EP17164317.4A Active EP3225195B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de desserrage
EP17164325.7A Pending EP3225182A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical
EP17164075.8A Active EP3238638B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant une commande de charge
EP17164120.2A Withdrawn EP3225180A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant une tige configurable
EP23202093.3A Pending EP4299018A3 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical
EP21153563.8A Pending EP3834745A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant un système de déclenchement rotatif
EP17164361.2A Active EP3225197B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de cartouche usagée
EP17164426.3A Active EP3228261B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un écran incluant un champ d'affichage ré-orientable
EP17164216.8A Active EP3225193B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de fixation de mâchoire
EP17164394.3A Active EP3225199B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant une mâchoire de blocage de fermeture

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EP17164408.1A Active EP3225184B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant un système de déclenchement rotatif
EP20150529.4A Active EP3656315B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant une mâchoire de blocage de fermeture

Family Applications After (20)

Application Number Title Priority Date Filing Date
EP17164433.9A Active EP3238639B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical conçu pour réaliser une coupe sélective de tissus
EP21214545.2A Pending EP3988035A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de cartouche usagée
EP19203275.3A Pending EP3616630A1 (fr) 2016-04-01 2017-03-31 Cartouches d'agrafes ayant des éléments atraumatiques
EP18208037.4A Pending EP3461424A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical modulaire comprenant un dispositif d'affichage
EP17164294.5A Active EP3225194B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de compression de tissu
EP20176510.4A Pending EP3718487A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un écran incluant un champ d'affichage ré-orientable
EP23199750.3A Pending EP4275626A3 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant une commande de charge
EP17164088.1A Active EP3225176B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical modulaire comprenant un dispositif d'affichage
EP19217086.8A Pending EP3656316A3 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de fixation de mâchoire
EP17164406.5A Active EP3225198B1 (fr) 2016-04-01 2017-03-31 Cartouches d'agrafes ayant des caractéristiques atraumatiques
EP17164317.4A Active EP3225195B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de desserrage
EP17164325.7A Pending EP3225182A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical
EP17164075.8A Active EP3238638B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant une commande de charge
EP17164120.2A Withdrawn EP3225180A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant une tige configurable
EP23202093.3A Pending EP4299018A3 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical
EP21153563.8A Pending EP3834745A1 (fr) 2016-04-01 2017-03-31 Système d'agrafage circulaire comprenant un système de déclenchement rotatif
EP17164361.2A Active EP3225197B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de cartouche usagée
EP17164426.3A Active EP3228261B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un écran incluant un champ d'affichage ré-orientable
EP17164216.8A Active EP3225193B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant un verrouillage de fixation de mâchoire
EP17164394.3A Active EP3225199B1 (fr) 2016-04-01 2017-03-31 Système d'agrafage chirurgical comprenant une mâchoire de blocage de fermeture

Country Status (6)

Country Link
US (16) US10456140B2 (fr)
EP (23) EP3225184B1 (fr)
JP (2) JP6938532B2 (fr)
CN (2) CN109310417B (fr)
BR (2) BR112018069861B1 (fr)
WO (15) WO2017172582A1 (fr)

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US10856867B2 (en) 2020-12-08
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